Organic electroluminescent materials and devices

ABSTRACT

Provided is a compound including a first ligand LA of Formula IIn Formula I, ring C is a 5- or 6-membered ring; each of X1 to X8 is C or N; one of X1 to X4 is C and is connected to ring C, and one of X1 to X4 is N and is coordinated to a metal M; Y is a divalent linker; K is a direct bond, O, or S; each R′, R″, RA, RB, and RC is hydrogen or a general substituent; at least one of RA or RB comprises an electron-withdrawing group; at least one of RB is a cyclic group; and metal M is selected from Os, Ir, Pd, Pt, Cu, Ag, and Au. Formulations, devices, and consumer products comprising the compound are also disclosed.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority under 35 U.S.C. § 119(e) to U.S. Provisional Application No. 63/196,866, filed on Jun. 4, 2021, the entire contents of which are incorporated herein by reference.

FIELD

The present disclosure generally relates to organometallic compounds and formulations and their various uses including as emitters in devices such as organic light emitting diodes and related electronic devices.

BACKGROUND

Opto-electronic devices that make use of organic materials are becoming increasingly desirable for various reasons. Many of the materials used to make such devices are relatively inexpensive, so organic opto-electronic devices have the potential for cost advantages over inorganic devices. In addition, the inherent properties of organic materials, such as their flexibility, may make them well suited for particular applications such as fabrication on a flexible substrate. Examples of organic opto-electronic devices include organic light emitting diodes/devices (OLEDs), organic phototransistors, organic photovoltaic cells, and organic photodetectors. For OLEDs, the organic materials may have performance advantages over conventional materials.

OLEDs make use of thin organic films that emit light when voltage is applied across the device. OLEDs are becoming an increasingly interesting technology for use in applications such as flat panel displays, illumination, and backlighting.

One application for phosphorescent emissive molecules is a full color display. Industry standards for such a display call for pixels adapted to emit particular colors, referred to as “saturated” colors. In particular, these standards call for saturated red, green, and blue pixels. Alternatively, the OLED can be designed to emit white light. In conventional liquid crystal displays emission from a white backlight is filtered using absorption filters to produce red, green and blue emission. The same technique can also be used with OLEDs. The white OLED can be either a single emissive layer (EML) device or a stack structure. Color may be measured using CIE coordinates, which are well known to the art.

SUMMARY

In one aspect, the present disclosure provides a compound comprising a first ligand L_(A) of Formula I,

wherein:

ring C is a 5-membered or 6-membered carbocyclic or heterocyclic ring;

each of X¹ to X⁸ is independently C or N;

one of X¹ to X⁴ is C and is connected to ring C, and one of X¹ to X⁴ is N and is coordinated to a metal M;

Y is selected from the group consisting of O, S, Se, NR′, BR′, BR′R″, CR′R″, SiR′R″, GeR′R″, C═O, C═CRR′, and C═NR′;

K is selected from the group consisting of a direct bond, O, and S;

each of R^(A), R^(B), and R^(C) independently represents mono to the maximum allowable substitution, or no substitution;

each R′, R″, R^(A), R^(B), and R^(C) is independently a hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, boryl, arylalkyl, alkoxy, aryloxy, amino, silyl, germyl, selenyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;

at least one of R^(A) or R^(B) comprises an electron-withdrawing group;

at least one of R^(B) is a cyclic group;

L_(A) is coordinated to a metal M via the indicated dashed lines;

metal M is selected from the group consisting of Os, Ir, Pd, Pt, Cu, Ag, and Au;

L_(A) can be joined with other ligands to comprise a tridentate, tetradentate, pentadentate, and hexadentate ligand; and

any two substituents can be joined or fused to form a ring.

In another aspect, the present disclosure provides a formulation of a compound having a first ligand of Formula I as described herein.

In yet another aspect, the present disclosure provides an OLED having an organic layer comprising a compound having a first ligand of Formula I as described herein.

In yet another aspect, the present disclosure provides a consumer product comprising an OLED with an organic layer comprising a compound having a first ligand of Formula I as described herein.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows an organic light emitting device.

FIG. 2 shows an inverted organic light emitting device that does not have a separate electron transport layer.

DETAILED DESCRIPTION A. Terminology

Unless otherwise specified, the below terms used herein are defined as follows:

As used herein, the term “organic” includes polymeric materials as well as small molecule organic materials that may be used to fabricate organic opto-electronic devices. “Small molecule” refers to any organic material that is not a polymer, and “small molecules” may actually be quite large. Small molecules may include repeat units in some circumstances. For example, using a long chain alkyl group as a substituent does not remove a molecule from the “small molecule” class. Small molecules may also be incorporated into polymers, for example as a pendent group on a polymer backbone or as a part of the backbone. Small molecules may also serve as the core moiety of a dendrimer, which consists of a series of chemical shells built on the core moiety. The core moiety of a dendrimer may be a fluorescent or phosphorescent small molecule emitter. A dendrimer may be a “small molecule,” and it is believed that all dendrimers currently used in the field of OLEDs are small molecules.

As used herein, “top” means furthest away from the substrate, while “bottom” means closest to the substrate. Where a first layer is described as “disposed over” a second layer, the first layer is disposed further away from substrate. There may be other layers between the first and second layer, unless it is specified that the first layer is “in contact with” the second layer. For example, a cathode may be described as “disposed over” an anode, even though there are various organic layers in between.

As used herein, “solution processable” means capable of being dissolved, dispersed, or transported in and/or deposited from a liquid medium, either in solution or suspension form.

A ligand may be referred to as “photoactive” when it is believed that the ligand directly contributes to the photoactive properties of an emissive material. A ligand may be referred to as “ancillary” when it is believed that the ligand does not contribute to the photoactive properties of an emissive material, although an ancillary ligand may alter the properties of a photoactive ligand.

As used herein, and as would be generally understood by one skilled in the art, a first “Highest Occupied Molecular Orbital” (HOMO) or “Lowest Unoccupied Molecular Orbital” (LUMO) energy level is “greater than” or “higher than” a second HOMO or LUMO energy level if the first energy level is closer to the vacuum energy level. Since ionization potentials (IP) are measured as a negative energy relative to a vacuum level, a higher HOMO energy level corresponds to an IP having a smaller absolute value (an IP that is less negative). Similarly, a higher LUMO energy level corresponds to an electron affinity (EA) having a smaller absolute value (an EA that is less negative). On a conventional energy level diagram, with the vacuum level at the top, the LUMO energy level of a material is higher than the HOMO energy level of the same material. A “higher” HOMO or LUMO energy level appears closer to the top of such a diagram than a “lower” HOMO or LUMO energy level.

As used herein, and as would be generally understood by one skilled in the art, a first work function is “greater than” or “higher than” a second work function if the first work function has a higher absolute value. Because work functions are generally measured as negative numbers relative to vacuum level, this means that a “higher” work function is more negative. On a conventional energy level diagram, with the vacuum level at the top, a “higher” work function is illustrated as further away from the vacuum level in the downward direction. Thus, the definitions of HOMO and LUMO energy levels follow a different convention than work functions.

The terms “halo,” “halogen,” and “halide” are used interchangeably and refer to fluorine, chlorine, bromine, and iodine.

The term “acyl” refers to a substituted carbonyl radical (C(O)—R_(s)).

The term “ester” refers to a substituted oxycarbonyl (—O—C(O)—R_(s) or —C(O)—O—R_(s)) radical.

The term “ether” refers to an —OR_(s) radical.

The terms “sulfanyl” or “thio-ether” are used interchangeably and refer to a —SR_(s) radical.

The term “selenyl” refers to a —SeR_(s) radical.

The term “sulfinyl” refers to a —S(O)—R_(s) radical.

The term “sulfonyl” refers to a —SO₂—R_(s) radical.

The term “phosphino” refers to a —P(R_(s))₃ radical, wherein each R_(s) can be same or different.

The term “silyl” refers to a —Si(R_(s))₃ radical, wherein each R_(s) can be same or different.

The term “germyl” refers to a —Ge(R_(s))₃ radical, wherein each R_(s) can be same or different.

The term “boryl” refers to a —B(R_(s))₂ radical or its Lewis adduct —B(R_(s))₃ radical, wherein R_(s) can be same or different.

In each of the above, R_(s) can be hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, and combination thereof. Preferred R_(s) is selected from the group consisting of alkyl, cycloalkyl, aryl, heteroaryl, and combination thereof.

The term “alkyl” refers to and includes both straight and branched chain alkyl radicals. Preferred alkyl groups are those containing from one to fifteen carbon atoms and includes methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, and the like. Additionally, the alkyl group may be optionally substituted.

The term “cycloalkyl” refers to and includes monocyclic, polycyclic, and spiro alkyl radicals. Preferred cycloalkyl groups are those containing 3 to 12 ring carbon atoms and includes cyclopropyl, cyclopentyl, cyclohexyl, bicyclo[3.1.1]heptyl, spiro[4.5]decyl, spiro[5.5]undecyl, adamantyl, and the like. Additionally, the cycloalkyl group may be optionally substituted.

The terms “heteroalkyl” or “heterocycloalkyl” refer to an alkyl or a cycloalkyl radical, respectively, having at least one carbon atom replaced by a heteroatom. Optionally the at least one heteroatom is selected from O, S, N, P, B, Si and Se, preferably, O, S or N. Additionally, the heteroalkyl or heterocycloalkyl group may be optionally substituted.

The term “alkenyl” refers to and includes both straight and branched chain alkene radicals. Alkenyl groups are essentially alkyl groups that include at least one carbon-carbon double bond in the alkyl chain. Cycloalkenyl groups are essentially cycloalkyl groups that include at least one carbon-carbon double bond in the cycloalkyl ring. The term “heteroalkenyl” as used herein refers to an alkenyl radical having at least one carbon atom replaced by a heteroatom. Optionally the at least one heteroatom is selected from O, S, N, P, B, Si, and Se, preferably, O, S, or N. Preferred alkenyl, cycloalkenyl, or heteroalkenyl groups are those containing two to fifteen carbon atoms. Additionally, the alkenyl, cycloalkenyl, or heteroalkenyl group may be optionally substituted.

The term “alkynyl” refers to and includes both straight and branched chain alkyne radicals. Alkynyl groups are essentially alkyl groups that include at least one carbon-carbon triple bond in the alkyl chain. Preferred alkynyl groups are those containing two to fifteen carbon atoms. Additionally, the alkynyl group may be optionally substituted.

The terms “aralkyl” or “arylalkyl” are used interchangeably and refer to an alkyl group that is substituted with an aryl group. Additionally, the aralkyl group may be optionally substituted.

The term “heterocyclic group” refers to and includes aromatic and non-aromatic cyclic radicals containing at least one heteroatom. Optionally the at least one heteroatom is selected from O, S, N, P, B, Si, and Se, preferably, O, S, or N. Heteroaromatic cyclic radicals may be used interchangeably with heteroaryl. Preferred hetero-non-aromatic cyclic groups are those containing 3 to 7 ring atoms which includes at least one hetero atom, and includes cyclic amines such as morpholino, piperidino, pyrrolidino, and the like, and cyclic ethers/thio-ethers, such as tetrahydrofuran, tetrahydropyran, tetrahydrothiophene, and the like. Additionally, the heterocyclic group may be optionally substituted.

The term “aryl” refers to and includes both single-ring aromatic hydrocarbyl groups and polycyclic aromatic ring systems. The polycyclic rings may have two or more rings in which two carbons are common to two adjoining rings (the rings are “fused”) wherein at least one of the rings is an aromatic hydrocarbyl group, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles, and/or heteroaryls. Preferred aryl groups are those containing six to thirty carbon atoms, preferably six to twenty carbon atoms, more preferably six to twelve carbon atoms. Especially preferred is an aryl group having six carbons, ten carbons or twelve carbons. Suitable aryl groups include phenyl, biphenyl, triphenyl, triphenylene, tetraphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene, preferably phenyl, biphenyl, triphenyl, triphenylene, fluorene, and naphthalene. Additionally, the aryl group may be optionally substituted.

The term “heteroaryl” refers to and includes both single-ring aromatic groups and polycyclic aromatic ring systems that include at least one heteroatom. The heteroatoms include, but are not limited to O, S, N, P, B, Si, and Se. In many instances, O, S, or N are the preferred heteroatoms. Hetero-single ring aromatic systems are preferably single rings with 5 or 6 ring atoms, and the ring can have from one to six heteroatoms. The hetero-polycyclic ring systems can have two or more rings in which two atoms are common to two adjoining rings (the rings are “fused”) wherein at least one of the rings is a heteroaryl, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles, and/or heteroaryls. The hetero-polycyclic aromatic ring systems can have from one to six heteroatoms per ring of the polycyclic aromatic ring system. Preferred heteroaryl groups are those containing three to thirty carbon atoms, preferably three to twenty carbon atoms, more preferably three to twelve carbon atoms. Suitable heteroaryl groups include dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine, preferably dibenzothiophene, dibenzofuran, dibenzoselenophene, carbazole, indolocarbazole, imidazole, pyridine, triazine, benzimidazole, 1,2-azaborine, 1,3-azaborine, 1,4-azaborine, borazine, and aza-analogs thereof. Additionally, the heteroaryl group may be optionally substituted.

Of the aryl and heteroaryl groups listed above, the groups of triphenylene, naphthalene, anthracene, dibenzothiophene, dibenzofuran, dibenzoselenophene, carbazole, indolocarbazole, imidazole, pyridine, pyrazine, pyrimidine, triazine, and benzimidazole, and the respective aza-analogs of each thereof are of particular interest.

The terms alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aralkyl, heterocyclic group, aryl, and heteroaryl, as used herein, are independently unsubstituted, or independently substituted, with one or more general substituents.

In many instances, the general substituents are selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, germyl, boryl, selenyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.

In some instances, the preferred general substituents are selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile, isonitrile, sulfanyl, and combinations thereof.

In some instances, the more preferred general substituents are selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, alkoxy, aryloxy, amino, silyl, boryl, aryl, heteroaryl, sulfanyl, and combinations thereof.

In yet other instances, the most preferred general substituents are selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, aryl, heteroaryl, and combinations thereof.

The terms “substituted” and “substitution” refer to a substituent other than H that is bonded to the relevant position, e.g., a carbon or nitrogen. For example, when R¹ represents mono-substitution, then one R¹ must be other than H (i.e., a substitution). Similarly, when R¹ represents di-substitution, then two of R¹ must be other than H. Similarly, when R¹ represents zero or no substitution, R¹, for example, can be a hydrogen for available valencies of ring atoms, as in carbon atoms for benzene and the nitrogen atom in pyrrole, or simply represents nothing for ring atoms with fully filled valencies, e.g., the nitrogen atom in pyridine. The maximum number of substitutions possible in a ring structure will depend on the total number of available valencies in the ring atoms.

As used herein, “combinations thereof” indicates that one or more members of the applicable list are combined to form a known or chemically stable arrangement that one of ordinary skill in the art can envision from the applicable list. For example, an alkyl and deuterium can be combined to form a partial or fully deuterated alkyl group; a halogen and alkyl can be combined to form a halogenated alkyl substituent; and a halogen, alkyl, and aryl can be combined to form a halogenated arylalkyl. In one instance, the term substitution includes a combination of two to four of the listed groups. In another instance, the term substitution includes a combination of two to three groups. In yet another instance, the term substitution includes a combination of two groups. Preferred combinations of substituent groups are those that contain up to fifty atoms that are not hydrogen or deuterium, or those which include up to forty atoms that are not hydrogen or deuterium, or those that include up to thirty atoms that are not hydrogen or deuterium. In many instances, a preferred combination of substituent groups will include up to twenty atoms that are not hydrogen or deuterium.

The “aza” designation in the fragments described herein, i.e. aza-dibenzofuran, aza-dibenzothiophene, etc. means that one or more of the C—H groups in the respective aromatic ring can be replaced by a nitrogen atom, for example, and without any limitation, azatriphenylene encompasses both dibenzo[f,h]quinoxaline and dibenzo[f,h]quinoline. One of ordinary skill in the art can readily envision other nitrogen analogs of the aza-derivatives described above, and all such analogs are intended to be encompassed by the terms as set forth herein.

As used herein, “deuterium” refers to an isotope of hydrogen. Deuterated compounds can be readily prepared using methods known in the art. For example, U.S. Pat. No. 8,557,400, Patent Pub. No. WO 2006/095951, and U.S. Pat. Application Pub. No. US 2011/0037057, which are hereby incorporated by reference in their entireties, describe the making of deuterium-substituted organometallic complexes. Further reference is made to Ming Yan, et al., Tetrahedron 2015, 71, 1425-30 and Atzrodt et al., Angew. Chem. Int. Ed. (Reviews) 2007, 46, 7744-65, which are incorporated by reference in their entireties, describe the deuteration of the methylene hydrogens in benzyl amines and efficient pathways to replace aromatic ring hydrogens with deuterium, respectively.

It is to be understood that when a molecular fragment is described as being a substituent or otherwise attached to another moiety, its name may be written as if it were a fragment (e.g. phenyl, phenylene, naphthyl, dibenzofuryl) or as if it were the whole molecule (e.g. benzene, naphthalene, dibenzofuran). As used herein, these different ways of designating a substituent or attached fragment are considered to be equivalent.

In some instance, a pair of adjacent substituents can be optionally joined or fused into a ring. The preferred ring is a five, six, or seven-membered carbocyclic or heterocyclic ring, includes both instances where the portion of the ring formed by the pair of substituents is saturated and where the portion of the ring formed by the pair of substituents is unsaturated. As used herein, “adjacent” means that the two substituents involved can be on the same ring next to each other, or on two neighboring rings having the two closest available substitutable positions, such as 2, 2′ positions in a biphenyl, or 1, 8 position in a naphthalene, as long as they can form a stable fused ring system.

B. The Compounds of the Present Disclosure

In one aspect, the present disclosure provides a compound comprising a first ligand L_(A) of Formula I

wherein:

ring C is a 5-membered or 6-membered carbocyclic or heterocyclic ring;

each of X¹ to X⁸ is independently C or N;

one of X¹ to X⁴ is C and is connected to ring C, and one of X¹ to X⁴ is N and is coordinated to a metal M;

Y is selected from the group consisting of O, S, Se, NR′, BR′, BR′R″, CR′R″, SiR′R″, GeR′R″, C═O, C═CRR′, and C═NR′;

K is selected from the group consisting of a direct bond, O, and S;

each of R^(A), R^(B), and R^(C) independently represents mono to the maximum allowable substitution, or no substitution;

each R′, R″, R^(A), R^(B), and R^(C) is independently a hydrogen or a substituent selected from the group consisting of the general substituents defined herein;

at least one of R^(A) or R^(B) comprises an electron-withdrawing group;

at least one of R^(B) is a cyclic group;

L_(A) is coordinated to a metal M via the indicated dashed lines;

metal M is selected from the group consisting of Os, Ir, Pd, Pt, Cu, Ag, and Au;

L_(A) can be joined with other ligands to comprise a tridentate, tetradentate, pentadentate, and hexadentate ligand; and any two substituents can be joined or fused to form a ring.

In some embodiments, when an R^(B) comprises an electron-withdrawing group, a different R^(B) is a cyclic group. In some embodiments, at least one R^(A) or R^(B) is an electron-withdrawing group.

In some embodiments, each R′, R″, R^(A), R^(B), and R^(C) is independently a hydrogen or a substituent selected from the group consisting of the preferred general substituents defined herein. In some embodiments, each R′, R″, R^(A), R^(B), and R^(C) is independently a hydrogen or a substituent selected from the group consisting of the more preferred general substituents defined herein. In some embodiments, each R′, R″, R^(A), R^(B), and R^(C) is independently a hydrogen or a substituent selected from the group consisting of the most preferred general substituents defined herein.

In some embodiments, at least one R^(A) comprises an electron-withdrawing group. In some embodiments, exactly one R^(A) comprises an electron-withdrawing group. In some embodiments, no R^(B) comprises an electron-withdrawing group.

In some embodiments, at least one R^(B) comprises an electron-withdrawing group In some embodiments, no R^(A) comprises an electron-withdrawing group.

In some embodiments, the electron-withdrawing group is selected from the group consisting of F, CF₃, CN, COCH₃, CHO, COCF₃, COOMe, COOCF₃, NO₂, SF₃, SiF₃, PF₄, SF₅, OCF₃, SCF₃, SeCF₃, SOCF₃, SeOCF₃, SO₂F, SO₂CF₃, SeO₂CF₃, OSO₂CF₃, OSeO₂CF₃, OCN, SCN, SeCN, NC, ⁺N(R)₃, (R)₂CCN, (R)₂CCF₃, CNC(CF₃)₂,

wherein each R is independently a hydrogen or a substituent selected from the group consisting of the General Substituents defined herein.

In some embodiments, the electron-withdrawing group is selected from the group consisting of fluoride, perfluoroalkyl, perfluorocycloalkyl, perfluorovinyl, CN, SCN, SF₅, and SCF₃.

In some embodiments, the R^(B) attached to X⁸ is an electron-withdrawing group. In some embodiments, the R^(B) attached to X⁷ is an electron-withdrawing group. In some embodiments, the R^(B) attached to X⁶ is an electron-withdrawing group. In some embodiments, the R^(B) attached to X⁵ is an electron-withdrawing group.

In some embodiments, the R^(A) attached to X⁴ is an electron-withdrawing group. In some embodiments, the R^(A) attached to X³ is an electron-withdrawing group. In some embodiments, the R^(A) attached to X² is an electron-withdrawing group. In some embodiments, the R^(A) attached to X¹ is an electron-withdrawing group.

In some embodiments, each of X¹ to X⁸ that is not coordinated to metal M is C.

In some embodiments, each of X¹ to X⁴ that is not coordinated to metal M is C.

In some embodiments, each of X⁵ to X⁸ is C.

In some embodiments, one of X¹ to X⁸ that is not coordinated to metal M is N.

In some embodiments, one of X⁵ to X⁸ is N.

In some embodiments, at least one R^(B) is a pendant cyclic group. In some such embodiments, the pendant cyclic group comprises at least one 5-membered or 6-membered carbocyclic or heterocyclic ring. In some such embodiments, the pendant cyclic group is a monocyclic group, which can be further substituted. In some such embodiments, the pendant cyclic group is a polycyclic group, which can be further substituted.

In some embodiments, R^(B) attached to X⁸ is a pendant cyclic group. In some embodiments, R^(B) attached to X⁷ is a pendant cyclic group. In some embodiments, R^(B) attached to X⁶ is a pendant cyclic group. In some embodiments, R^(B) attached to X⁵ is a pendant cyclic group.

In some embodiments, R^(B) attached to X⁷ is a cyclic group and R^(B) attached to X⁸ is an electron-withdrawing group.

In some embodiments, each R^(B) that is not a cyclic group or an electron-withdrawing group is hydrogen, and each R^(A) that is not an electron-withdrawing group is hydrogen.

In some embodiments, two R^(B) are joined or fused to form the cyclic group. In some such embodiments, the cyclic group comprises an electron-withdrawing group. In some such embodiments, the cyclic group is non-aromatic. In some such embodiments, the cyclic group is aromatic.

In some embodiments, ring C is a 6-membered aryl or heteroaryl ring.

In some embodiments, ring C is a 5-membered heteroaryl ring. In some embodiments, ring C is selected from the group consisting of benzene, pyridine, pyrimidine, pyridazine, pyrazine, triazine, imidazole, pyrazole, pyrrole, oxazole, furan, thiophene, and thiazole.

In some embodiments, two R^(C) are joined to form a ring fused to ring C. In some such embodiments, the ring fused to ring C is a 5-membered or 6-membered aromatic ring. In some such embodiments, the ring fused to ring C is selected from the group consisting of benzene, pyridine, pyrimidine, pyridazine, pyrazine, triazine, imidazole, pyrazole, pyrrole, oxazole, furan, thiophene, and thiazole.

In some embodiments, two R^(C) are joined to form a polycyclic fused ring structure.

In some embodiments, the ligand L_(A) is selected from the group consisting of:

In some embodiments, the ligand L_(A) is selected from the group consisting of the structures of the following LIST 17:

wherein Y² is selected from the group consisting of O, S, Se, NR^(Y′), BR^(Y′), BR^(Y′)R^(Y″), CR^(Y′)R^(Y″), SiR^(Y′)R^(Y″), GeR^(Y′)R^(Y″), C═O, C═CR^(Y′)R^(Y″), and C═NR^(Y′), and

wherein each of R^(Y′) and R^(Y) is independently a hydrogen or a substituent selected from the group consisting of the preferred general substituents.

In some embodiments, the ligand L_(A) is selected from the group consisting of: L_(Ai-m-X), where i is an integer from 1 to 2964, m is an integer from 1 to 52, and X is an integer from 1 to 4, where X=1 represents O, X=2 represents S, X=3 represents NCH₃, and X=4 represents Se;

wherein each of L_(Ai-1-X) to L_(Ai-52-X) has a structure in the following LIST 1:

wherein, for each i from 1 to 2964, R^(E) and G are defined by the following LIST 2:

i R^(E) G i R^(E) G i R^(E) G i R^(E) G 1 R¹ G¹ 2 R¹ G² 3 R¹ G³ 4 R¹ G⁴ 5 R² G¹ 6 R² G² 7 R² G³ 8 R² G⁴ 9 R³ G¹ 10 R³ G² 11 R³ G³ 12 R³ G⁴ 13 R⁴ G¹ 14 R⁴ G² 15 R⁴ G³ 16 R⁴ G⁴ 17 R⁵ G¹ 18 R⁵ G² 19 R⁵ G³ 20 R⁵ G⁴ 21 R⁶ G¹ 22 R⁶ G² 23 R⁶ G³ 24 R⁶ G⁴ 25 R⁷ G¹ 26 R⁷ G² 27 R⁷ G³ 28 R⁷ G⁴ 29 R⁸ G¹ 30 R⁸ G² 31 R⁸ G³ 32 R⁸ G⁴ 33 R⁹ G¹ 34 R⁹ G² 35 R⁹ G³ 36 R⁹ G⁴ 37 R¹⁰ G¹ 38 R¹⁰ G² 39 R¹⁰ G³ 40 R¹⁰ G⁴ 41 R¹¹ G¹ 42 R¹¹ G² 43 R¹¹ G³ 44 R¹¹ G⁴ 45 R¹² G¹ 46 R¹² G² 47 R¹² G³ 48 R¹² G⁴ 49 R¹³ G¹ 50 R¹³ G² 51 R¹³ G³ 52 R¹³ G⁴ 53 R¹⁴ G¹ 54 R¹⁴ G² 55 R¹⁴ G³ 56 R¹⁴ G⁴ 57 R¹⁵ G¹ 58 R¹⁵ G² 59 R¹⁵ G³ 60 R¹⁵ G⁴ 61 R¹⁶ G¹ 62 R¹⁶ G² 63 R¹⁶ G³ 64 R¹⁶ G⁴ 65 R¹⁷ G¹ 66 R¹⁷ G² 67 R¹⁷ G³ 68 R¹⁷ G⁴ 69 R¹⁸ G¹ 70 R¹⁸ G² 71 R¹⁸ G³ 72 R¹⁸ G⁴ 73 R¹⁹ G¹ 74 R¹⁹ G² 75 R¹⁹ G³ 76 R¹⁹ G⁴ 77 R²⁰ G¹ 78 R²⁰ G² 79 R²⁰ G³ 80 R²⁰ G⁴ 81 R²¹ G¹ 82 R²¹ G² 83 R²¹ G³ 84 R²¹ G⁴ 85 R²² G¹ 86 R²² G² 87 R²² G³ 88 R²² G⁴ 89 R²³ G¹ 90 R²³ G² 91 R²³ G³ 92 R²³ G⁴ 93 R²⁴ G¹ 94 R²⁴ G² 95 R²⁴ G³ 96 R²⁴ G⁴ 97 R²⁵ G¹ 98 R²⁵ G² 99 R²⁵ G³ 100 R²⁵ G⁴ 101 R²⁶ G¹ 102 R²⁶ G² 103 R²⁶ G³ 104 R²⁶ G⁴ 105 R²⁷ G¹ 106 R²⁷ G² 107 R²⁷ G³ 108 R²⁷ G⁴ 109 R²⁸ G¹ 110 R²⁸ G² 111 R²⁸ G³ 112 R²⁸ G⁴ 113 R²⁹ G¹ 114 R²⁹ G² 115 R²⁹ G³ 116 R²⁹ G⁴ 117 R³⁰ G¹ 118 R³⁰ G² 119 R³⁰ G³ 120 R³⁰ G⁴ 121 R³¹ G¹ 122 R³¹ G² 123 R³¹ G³ 124 R³¹ G⁴ 125 R³² G¹ 126 R³² G² 127 R³² G³ 128 R³² G⁴ 129 R³³ G¹ 130 R³³ G² 131 R³³ G³ 132 R³³ G⁴ 133 R³⁴ G¹ 134 R³⁴ G² 135 R³⁴ G³ 136 R³⁴ G⁴ 137 R³⁵ G¹ 138 R³⁵ G² 139 R³⁵ G³ 140 R³⁵ G⁴ 141 R³⁶ G¹ 142 R³⁶ G² 143 R³⁶ G³ 144 R³⁶ G⁴ 145 R³⁷ G¹ 146 R³⁷ G² 147 R³⁷ G³ 148 R³⁷ G⁴ 149 R³⁸ G¹ 150 R³⁸ G² 151 R³⁸ G³ 152 R³⁸ G⁴ 153 R³⁹ G¹ 154 R³⁹ G² 155 R³⁹ G³ 156 R³⁹ G⁴ 157 R⁴⁰ G¹ 158 R⁴⁰ G² 159 R⁴⁰ G³ 160 R⁴⁰ G⁴ 161 R⁴¹ G¹ 162 R⁴¹ G² 163 R⁴¹ G³ 164 R⁴¹ G⁴ 165 R⁴² G¹ 166 R⁴² G² 167 R⁴² G³ 168 R⁴² G⁴ 169 R⁴³ G¹ 170 R⁴³ G² 171 R⁴³ G³ 172 R⁴³ G⁴ 173 R⁴⁴ G¹ 174 R⁴⁴ G² 175 R⁴⁴ G³ 176 R⁴⁴ G⁴ 177 R⁴⁵ G¹ 178 R⁴⁵ G² 179 R⁴⁵ G³ 180 R⁴⁵ G⁴ 181 R⁴⁶ G¹ 182 R⁴⁶ G² 183 R⁴⁶ G³ 184 R⁴⁶ G⁴ 185 R⁴⁷ G¹ 186 R⁴⁷ G² 187 R⁴⁷ G³ 188 R⁴⁷ G⁴ 189 R⁴⁸ G¹ 190 R⁴⁸ G² 191 R⁴⁸ G³ 192 R⁴⁸ G⁴ 193 R⁴⁹ G¹ 194 R⁴⁹ G² 195 R⁴⁹ G³ 196 R⁴⁹ G⁴ 197 R⁵⁰ G¹ 198 R⁵⁰ G² 199 R⁵⁰ G³ 200 R⁵⁰ G⁴ 201 R⁵¹ G¹ 202 R⁵¹ G² 203 R⁵¹ G³ 204 R⁵¹ G⁴ 205 R⁵² G¹ 206 R⁵² G² 207 R⁵² G³ 208 R⁵² G⁴ 209 R⁵³ G¹ 210 R⁵³ G² 211 R⁵³ G³ 212 R⁵³ G⁴ 213 R⁵⁴ G¹ 214 R⁵⁴ G² 215 R⁵⁴ G³ 216 R⁵⁴ G⁴ 217 R⁵⁵ G¹ 218 R⁵⁵ G² 219 R⁵⁵ G³ 220 R⁵⁵ G⁴ 221 R⁵⁶ G¹ 222 R⁵⁶ G² 223 R⁵⁶ G³ 224 R⁵⁶ G⁴ 225 R⁵⁷ G¹ 226 R⁵⁷ G² 227 R⁵⁷ G³ 228 R⁵⁷ G⁴ 229 R¹ G⁵ 230 R¹ G⁶ 231 R¹ G⁷ 232 R¹ G⁸ 233 R² G⁵ 234 R² G⁶ 235 R² G⁷ 236 R² G⁸ 237 R³ G⁵ 238 R³ G⁶ 239 R³ G⁷ 240 R³ G⁸ 241 R⁴ G⁵ 242 R⁴ G⁶ 243 R⁴ G⁷ 244 R⁴ G⁸ 245 R⁵ G⁵ 246 R⁵ G⁶ 247 R⁵ G⁷ 248 R⁵ G⁸ 249 R⁶ G⁵ 250 R⁶ G⁶ 251 R⁶ G⁷ 252 R⁶ G⁸ 253 R⁷ G⁵ 254 R⁷ G⁶ 255 R⁷ G⁷ 256 R⁷ G⁸ 257 R⁸ G⁵ 258 R⁸ G⁶ 259 R⁸ G⁷ 260 R⁸ G⁸ 261 R⁹ G⁵ 262 R⁹ G⁶ 263 R⁹ G⁷ 264 R⁹ G⁸ 265 R¹⁰ G⁵ 266 R¹⁰ G⁶ 267 R¹⁰ G⁷ 268 R¹⁰ G⁸ 269 R¹¹ G⁵ 270 R¹¹ G⁶ 271 R¹¹ G⁷ 272 R¹¹ G⁸ 273 R¹² G⁵ 274 R¹² G⁶ 275 R¹² G⁷ 276 R¹² G⁸ 277 R¹³ G⁵ 278 R¹³ G⁶ 279 R¹³ G⁷ 280 R¹³ G⁸ 281 R¹⁴ G⁵ 282 R¹⁴ G⁶ 283 R¹⁴ G⁷ 284 R¹⁴ G⁸ 285 R¹⁵ G⁵ 286 R¹⁵ G⁶ 287 R¹⁵ G⁷ 288 R¹⁵ G⁸ 289 R¹⁶ G⁵ 290 R¹⁶ G⁶ 291 R¹⁶ G⁷ 292 R¹⁶ G⁸ 293 R¹⁷ G⁵ 294 R¹⁷ G⁶ 295 R¹⁷ G⁷ 296 R¹⁷ G⁸ 297 R¹⁸ G⁵ 298 R¹⁸ G⁶ 299 R¹⁸ G⁷ 300 R¹⁸ G⁸ 301 R¹⁹ G⁵ 302 R¹⁹ G⁶ 303 R¹⁹ G⁷ 304 R¹⁹ G⁸ 305 R²⁰ G⁵ 306 R²⁰ G⁶ 307 R²⁰ G⁷ 308 R²⁰ G⁸ 309 R²¹ G⁵ 310 R²¹ G⁶ 311 R²¹ G⁷ 312 R²¹ G⁸ 313 R²² G⁵ 314 R²² G⁶ 315 R²² G⁷ 316 R²² G⁸ 317 R²³ G⁵ 318 R²³ G⁶ 319 R²³ G⁷ 320 R²³ G⁸ 321 R²⁴ G⁵ 322 R²⁴ G⁶ 323 R²⁴ G⁷ 324 R²⁴ G⁸ 325 R²⁵ G⁵ 326 R²⁵ G⁶ 327 R²⁵ G⁷ 328 R²⁵ G⁸ 329 R²⁶ G⁵ 330 R²⁶ G⁶ 331 R²⁶ G⁷ 332 R²⁶ G⁸ 333 R²⁷ G⁵ 334 R²⁷ G⁶ 335 R²⁷ G⁷ 336 R²⁷ G⁸ 337 R²⁸ G⁵ 338 R²⁸ G⁶ 339 R²⁸ G⁷ 340 R²⁸ G⁸ 341 R²⁹ G⁵ 342 R²⁹ G⁶ 343 R²⁹ G⁷ 344 R²⁹ G⁸ 345 R³⁰ G⁵ 346 R³⁰ G⁶ 347 R³⁰ G⁷ 348 R³⁰ G⁸ 349 R³¹ G⁵ 350 R³¹ G⁶ 351 R³¹ G⁷ 352 R³¹ G⁸ 353 R³² G⁵ 354 R³² G⁶ 355 R³² G⁷ 356 R³² G⁸ 357 R³³ G⁵ 358 R³³ G⁶ 359 R³³ G⁷ 360 R³³ G⁸ 361 R³⁴ G⁵ 362 R³⁴ G⁶ 363 R³⁴ G⁷ 364 R³⁴ G⁸ 365 R³⁵ G⁵ 366 R³⁵ G⁶ 367 R³⁵ G⁷ 368 R³⁵ G⁸ 369 R³⁶ G⁵ 370 R³⁶ G⁶ 371 R³⁶ G⁷ 372 R³⁶ G⁸ 373 R³⁷ G⁵ 374 R³⁷ G⁶ 375 R³⁷ G⁷ 376 R³⁷ G⁸ 377 R³⁸ G⁵ 378 R³⁸ G⁶ 379 R³⁸ G⁷ 380 R³⁸ G⁸ 381 R³⁹ G⁵ 382 R³⁹ G⁶ 383 R³⁹ G⁷ 384 R³⁹ G⁸ 385 R⁴⁰ G⁵ 386 R⁴⁰ G⁶ 387 R⁴⁰ G⁷ 388 R⁴⁰ G⁸ 389 R⁴¹ G⁵ 390 R⁴¹ G⁶ 391 R⁴¹ G⁷ 392 R⁴¹ G⁸ 393 R⁴² G⁵ 394 R⁴² G⁶ 395 R⁴² G⁷ 396 R⁴² G⁸ 397 R⁴³ G⁵ 398 R⁴³ G⁶ 399 R⁴³ G⁷ 400 R⁴³ G⁸ 401 R⁴⁴ G⁵ 402 R⁴⁴ G⁶ 403 R⁴⁴ G⁷ 404 R⁴⁴ G⁸ 405 R⁴⁵ G⁵ 406 R⁴⁵ G⁶ 407 R⁴⁵ G⁷ 408 R⁴⁵ G⁸ 409 R⁴⁶ G⁵ 410 R⁴⁶ G⁶ 411 R⁴⁶ G⁷ 412 R⁴⁶ G⁸ 413 R⁴⁷ G⁵ 414 R⁴⁷ G⁶ 415 R⁴⁷ G⁷ 416 R⁴⁷ G⁸ 417 R⁴⁸ G⁵ 418 R⁴⁸ G⁶ 419 R⁴⁸ G⁷ 420 R⁴⁸ G⁸ 421 R⁴⁹ G⁵ 422 R⁴⁹ G⁶ 423 R⁴⁹ G⁷ 424 R⁴⁹ G⁸ 425 R⁵⁰ G⁵ 426 R⁵⁰ G⁶ 427 R⁵⁰ G⁷ 428 R⁵⁰ G⁸ 429 R⁵¹ G⁵ 430 R⁵¹ G⁶ 431 R⁵¹ G⁷ 432 R⁵¹ G⁸ 433 R⁵² G⁵ 434 R⁵² G⁶ 435 R⁵² G⁷ 436 R⁵² G⁸ 437 R⁵³ G⁵ 438 R⁵³ G⁶ 439 R⁵³ G⁷ 440 R⁵³ G⁸ 441 R⁵⁴ G⁵ 442 R⁵⁴ G⁶ 443 R⁵⁴ G⁷ 444 R⁵⁴ G⁸ 445 R⁵⁵ G⁵ 446 R⁵⁵ G⁶ 447 R⁵⁵ G⁷ 448 R⁵⁵ G⁸ 449 R⁵⁶ G⁵ 450 R⁵⁶ G⁶ 451 R⁵⁶ G⁷ 452 R⁵⁶ G⁸ 453 R⁵⁷ G⁵ 454 R⁵⁷ G⁶ 455 R⁵⁷ G⁷ 456 R⁵⁷ G⁸ 457 R¹ G⁹ 458 R¹ G¹⁰ 459 R¹ G¹¹ 460 R¹ G¹² 461 R² G⁹ 462 R² G¹⁰ 463 R² G¹¹ 464 R² G¹² 465 R³ G⁹ 466 R³ G¹⁰ 467 R³ G¹¹ 468 R³ G¹² 469 R⁴ G⁹ 470 R⁴ G¹⁰ 471 R⁴ G¹¹ 472 R⁴ G¹² 473 R⁵ G⁹ 474 R⁵ G¹⁰ 475 R⁵ G¹¹ 476 R⁵ G¹² 477 R⁶ G⁹ 478 R⁶ G¹⁰ 479 R⁶ G¹¹ 480 R⁶ G¹² 481 R⁷ G⁹ 482 R⁷ G¹⁰ 483 R⁷ G¹¹ 484 R⁷ G¹² 485 R⁸ G⁹ 486 R⁸ G¹⁰ 487 R⁸ G¹¹ 488 R⁸ G¹² 489 R⁹ G⁹ 490 R⁹ G¹⁰ 491 R⁹ G¹¹ 492 R⁹ G¹² 493 R¹⁰ G⁹ 494 R¹⁰ G¹⁰ 495 R¹⁰ G¹¹ 496 R¹⁰ G¹² 497 R¹¹ G⁹ 498 R¹¹ G¹⁰ 499 R¹¹ G¹¹ 500 R¹¹ G¹² 501 R¹² G⁹ 502 R¹² G¹⁰ 503 R¹² G¹¹ 504 R¹² G¹² 505 R¹³ G⁹ 506 R¹³ G¹⁰ 507 R¹³ G¹¹ 508 R¹³ G¹² 509 R¹⁴ G⁹ 510 R¹⁴ G¹⁰ 511 R¹⁴ G¹¹ 512 R¹⁴ G¹² 513 R¹⁵ G⁹ 514 R¹⁵ G¹⁰ 515 R¹⁵ G¹¹ 516 R¹⁵ G¹² 517 R¹⁶ G⁹ 518 R¹⁶ G¹⁰ 519 R¹⁶ G¹¹ 520 R¹⁶ G¹² 521 R¹⁷ G⁹ 522 R¹⁷ G¹⁰ 523 R¹⁷ G¹¹ 524 R¹⁷ G¹² 525 R¹⁸ G⁹ 526 R¹⁸ G¹⁰ 527 R¹⁸ G¹¹ 528 R¹⁸ G¹² 529 R¹⁹ G⁹ 530 R¹⁹ G¹⁰ 531 R¹⁹ G¹¹ 532 R¹⁹ G¹² 533 R²⁰ G⁹ 534 R²⁰ G¹⁰ 535 R²⁰ G¹¹ 536 R²⁰ G¹² 537 R²¹ G⁹ 538 R²¹ G¹⁰ 539 R²¹ G¹¹ 540 R²¹ G¹² 541 R²² G⁹ 542 R²² G¹⁰ 543 R²² G¹¹ 544 R²² G¹² 545 R²³ G⁹ 546 R²³ G¹⁰ 547 R²³ G¹¹ 548 R²³ G¹² 549 R²⁴ G⁹ 550 R²⁴ G¹⁰ 551 R²⁴ G¹¹ 552 R²⁴ G¹² 553 R²⁵ G⁹ 554 R²⁵ G¹⁰ 555 R²⁵ G¹¹ 556 R²⁵ G¹² 557 R²⁶ G⁹ 558 R²⁶ G¹⁰ 559 R²⁶ G¹¹ 560 R²⁶ G¹² 561 R²⁷ G⁹ 562 R²⁷ G¹⁰ 563 R²⁷ G¹¹ 564 R²⁷ G¹² 565 R²⁸ G⁹ 566 R²⁸ G¹⁰ 567 R²⁸ G¹¹ 568 R²⁸ G¹² 569 R²⁹ G⁹ 570 R²⁹ G¹⁰ 571 R²⁹ G¹¹ 572 R²⁹ G¹² 573 R³⁰ G⁹ 574 R³⁰ G¹⁰ 575 R³⁰ G¹¹ 576 R³⁰ G¹² 577 R³¹ G⁹ 578 R³¹ G¹⁰ 579 R³¹ G¹¹ 580 R³¹ G¹² 581 R³² G⁹ 582 R³² G¹⁰ 583 R³² G¹¹ 584 R³² G¹² 585 R³³ G⁹ 586 R³³ G¹⁰ 587 R³³ G¹¹ 588 R³³ G¹² 589 R³⁴ G⁹ 590 R³⁴ G¹⁰ 591 R³⁴ G¹¹ 592 R³⁴ G¹² 593 R³⁵ G⁹ 594 R³⁵ G¹⁰ 595 R³⁵ G¹¹ 596 R³⁵ G¹² 597 R³⁶ G⁹ 598 R³⁶ G¹⁰ 599 R³⁶ G¹¹ 600 R³⁶ G¹² 601 R³⁷ G⁹ 602 R³⁷ G¹⁰ 603 R³⁷ G¹¹ 604 R³⁷ G¹² 605 R³⁸ G⁹ 606 R³⁸ G¹⁰ 607 R³⁸ G¹¹ 608 R³⁸ G¹² 609 R³⁹ G⁹ 610 R³⁹ G¹⁰ 611 R³⁹ G¹¹ 612 R³⁹ G¹² 613 R⁴⁰ G⁹ 614 R⁴⁰ G¹⁰ 615 R⁴⁰ G¹¹ 616 R⁴⁰ G¹² 617 R⁴¹ G⁹ 618 R⁴¹ G¹⁰ 619 R⁴¹ G¹¹ 620 R⁴¹ G¹² 621 R⁴² G⁹ 622 R⁴² G¹⁰ 623 R⁴² G¹¹ 624 R⁴² G¹² 625 R⁴³ G⁹ 626 R⁴³ G¹⁰ 627 R⁴³ G¹¹ 628 R⁴³ G¹² 629 R⁴⁴ G⁹ 630 R⁴⁴ G¹⁰ 631 R⁴⁴ G¹¹ 632 R⁴⁴ G¹² 633 R⁴⁵ G⁹ 634 R⁴⁵ G¹⁰ 635 R⁴⁵ G¹¹ 636 R⁴⁵ G¹² 637 R⁴⁶ G⁹ 638 R⁴⁶ G¹⁰ 639 R⁴⁶ G¹¹ 640 R⁴⁶ G¹² 641 R⁴⁷ G⁹ 642 R⁴⁷ G¹⁰ 643 R⁴⁷ G¹¹ 644 R⁴⁷ G¹² 645 R⁴⁸ G⁹ 646 R⁴⁸ G¹⁰ 647 R⁴⁸ G¹¹ 648 R⁴⁸ G¹² 649 R⁴⁹ G⁹ 650 R⁴⁹ G¹⁰ 651 R⁴⁹ G¹¹ 652 R⁴⁹ G¹² 653 R⁵⁰ G⁹ 654 R⁵⁰ G¹⁰ 655 R⁵⁰ G¹¹ 656 R⁵⁰ G¹² 657 R⁵¹ G⁹ 658 R⁵¹ G¹⁰ 659 R⁵¹ G¹¹ 660 R⁵¹ G¹² 661 R⁵² G⁹ 662 R⁵² G¹⁰ 663 R⁵² G¹¹ 664 R⁵² G¹² 665 R⁵³ G⁹ 666 R⁵³ G¹⁰ 667 R⁵³ G¹¹ 668 R⁵³ G¹² 669 R⁵⁴ G⁹ 670 R⁵⁴ G¹⁰ 671 R⁵⁴ G¹¹ 672 R⁵⁴ G¹² 673 R⁵⁵ G⁹ 674 R⁵⁵ G¹⁰ 675 R⁵⁵ G¹¹ 676 R⁵⁵ G¹² 677 R⁵⁶ G⁹ 678 R⁵⁶ G¹⁰ 679 R⁵⁶ G¹¹ 680 R⁵⁶ G¹² 681 R⁵⁷ G⁹ 682 R⁵⁷ G¹⁰ 683 R⁵⁷ G¹¹ 684 R⁵⁷ G¹² 685 R¹ G¹³ 686 R¹ G¹⁴ 687 R¹ G¹⁵ 688 R¹ G¹⁶ 689 R² G¹³ 690 R² G¹⁴ 691 R² G¹⁵ 692 R² G¹⁶ 693 R³ G¹³ 694 R³ G¹⁴ 695 R³ G¹⁵ 696 R³ G¹⁶ 697 R⁴ G¹³ 698 R⁴ G¹⁴ 699 R⁴ G¹⁵ 700 R⁴ G¹⁶ 701 R⁵ G¹³ 702 R⁵ G¹⁴ 703 R⁵ G¹⁵ 704 R⁵ G¹⁶ 705 R⁶ G¹³ 706 R⁶ G¹⁴ 707 R⁶ G¹⁵ 708 R⁶ G¹⁶ 709 R⁷ G¹³ 710 R⁷ G¹⁴ 711 R⁷ G¹⁵ 712 R⁷ G¹⁶ 713 R⁸ G¹³ 714 R⁸ G¹⁴ 715 R⁸ G¹⁵ 716 R⁸ G¹⁶ 717 R⁹ G¹³ 718 R⁹ G¹⁴ 719 R⁹ G¹⁵ 720 R⁹ G¹⁶ 721 R¹⁰ G¹³ 722 R¹⁰ G¹⁴ 723 R¹⁰ G¹⁵ 724 R¹⁰ G¹⁶ 725 R¹¹ G¹³ 726 R¹¹ G¹⁴ 727 R¹¹ G¹⁵ 728 R¹¹ G¹⁶ 729 R¹² G¹³ 730 R¹² G¹⁴ 731 R¹² G¹⁵ 732 R¹² G¹⁶ 733 R¹³ G¹³ 734 R¹³ G¹⁴ 735 R¹³ G¹⁵ 736 R¹³ G¹⁶ 737 R¹⁴ G¹³ 738 R¹⁴ G¹⁴ 739 R¹⁴ G¹⁵ 740 R¹⁴ G¹⁶ 741 R¹⁵ G¹³ 742 R¹⁵ G¹⁴ 743 R¹⁵ G¹⁵ 744 R¹⁵ G¹⁶ 745 R¹⁶ G¹³ 746 R¹⁶ G¹⁴ 747 R¹⁶ G¹⁵ 748 R¹⁶ G¹⁶ 749 R¹⁷ G¹³ 750 R¹⁷ G¹⁴ 751 R¹⁷ G¹⁵ 752 R¹⁷ G¹⁶ 753 R¹⁸ G¹³ 754 R¹⁸ G¹⁴ 755 R¹⁸ G¹⁵ 756 R¹⁸ G¹⁶ 757 R¹⁹ G¹³ 758 R¹⁹ G¹⁴ 759 R¹⁹ G¹⁵ 760 R¹⁹ G¹⁶ 761 R²⁰ G¹³ 762 R²⁰ G¹⁴ 763 R²⁰ G¹⁵ 764 R²⁰ G¹⁶ 765 R²¹ G¹³ 766 R²¹ G¹⁴ 767 R²¹ G¹⁵ 768 R²¹ G¹⁶ 769 R²² G¹³ 770 R²² G¹⁴ 771 R²² G¹⁵ 772 R²² G¹⁶ 773 R²³ G¹³ 774 R²³ G¹⁴ 775 R²³ G¹⁵ 776 R²³ G¹⁶ 777 R²⁴ G¹³ 778 R²⁴ G¹⁴ 779 R²⁴ G¹⁵ 780 R²⁴ G¹⁶ 781 R²⁵ G¹³ 782 R²⁵ G¹⁴ 783 R²⁵ G¹⁵ 784 R²⁵ G¹⁶ 785 R²⁶ G¹³ 786 R²⁶ G¹⁴ 787 R²⁶ G¹⁵ 788 R²⁶ G¹⁶ 789 R²⁷ G¹³ 790 R²⁷ G¹⁴ 791 R²⁷ G¹⁵ 792 R²⁷ G¹⁶ 793 R²⁸ G¹³ 794 R²⁸ G¹⁴ 795 R²⁸ G¹⁵ 796 R²⁸ G¹⁶ 797 R²⁹ G¹³ 798 R²⁹ G¹⁴ 799 R²⁹ G¹⁵ 800 R²⁹ G¹⁶ 801 R³⁰ G¹³ 802 R³⁰ G¹⁴ 803 R³⁰ G¹⁵ 804 R³⁰ G¹⁶ 805 R³¹ G¹³ 806 R³¹ G¹⁴ 807 R³¹ G¹⁵ 808 R³¹ G¹⁶ 809 R³² G¹³ 810 R³² G¹⁴ 811 R³² G¹⁵ 812 R³² G¹⁶ 813 R³³ G¹³ 814 R³³ G¹⁴ 815 R³³ G¹⁵ 816 R³³ G¹⁶ 817 R³⁴ G¹³ 818 R³⁴ G¹⁴ 819 R³⁴ G¹⁵ 820 R³⁴ G¹⁶ 821 R³⁵ G¹³ 822 R³⁵ G¹⁴ 823 R³⁵ G¹⁵ 824 R³⁵ G¹⁶ 825 R³⁶ G¹³ 826 R³⁶ G¹⁴ 827 R³⁶ G¹⁵ 828 R³⁶ G¹⁶ 829 R³⁷ G¹³ 830 R³⁷ G¹⁴ 831 R³⁷ G¹⁵ 832 R³⁷ G¹⁶ 833 R³⁸ G¹³ 834 R³⁸ G¹⁴ 835 R³⁸ G¹⁵ 836 R³⁸ G¹⁶ 837 R³⁹ G¹³ 838 R³⁹ G¹⁴ 839 R³⁹ G¹⁵ 840 R³⁹ G¹⁶ 841 R⁴⁰ G¹³ 842 R⁴⁰ G¹⁴ 843 R⁴⁰ G¹⁵ 844 R⁴⁰ G¹⁶ 845 R⁴¹ G¹³ 846 R⁴¹ G¹⁴ 847 R⁴¹ G¹⁵ 848 R⁴¹ G¹⁶ 849 R⁴² G¹³ 850 R⁴² G¹⁴ 851 R⁴² G¹⁵ 852 R⁴² G¹⁶ 853 R⁴³ G¹³ 854 R⁴³ G¹⁴ 855 R⁴³ G¹⁵ 856 R⁴³ G¹⁶ 857 R⁴⁴ G¹³ 858 R⁴⁴ G¹⁴ 859 R⁴⁴ G¹⁵ 860 R⁴⁴ G¹⁶ 861 R⁴⁵ G¹³ 862 R⁴⁵ G¹⁴ 863 R⁴⁵ G¹⁵ 864 R⁴⁵ G¹⁶ 865 R⁴⁶ G¹³ 866 R⁴⁶ G¹⁴ 867 R⁴⁶ G¹⁵ 868 R⁴⁶ G¹⁶ 869 R⁴⁷ G¹³ 870 R⁴⁷ G¹⁴ 871 R⁴⁷ G¹⁵ 872 R⁴⁷ G¹⁶ 873 R⁴⁸ G¹³ 874 R⁴⁸ G¹⁴ 875 R⁴⁸ G¹⁵ 876 R⁴⁸ G¹⁶ 877 R⁴⁹ G¹³ 878 R⁴⁹ G¹⁴ 879 R⁴⁹ G¹⁵ 880 R⁴⁹ G¹⁶ 881 R⁵⁰ G¹³ 882 R⁵⁰ G¹⁴ 883 R⁵⁰ G¹⁵ 884 R⁵⁰ G¹⁶ 885 R⁵¹ G¹³ 886 R⁵¹ G¹⁴ 887 R⁵¹ G¹⁵ 888 R⁵¹ G¹⁶ 889 R⁵² G¹³ 890 R⁵² G¹⁴ 891 R⁵² G¹⁵ 892 R⁵² G¹⁶ 893 R⁵³ G¹³ 894 R⁵³ 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1216 R¹⁹ G²⁴ 1217 R²⁰ G²¹ 1218 R²⁰ G²² 1219 R²⁰ G²³ 1220 R²⁰ G²⁴ 1221 R²¹ G²¹ 1222 R²¹ G²² 1223 R²¹ G²³ 1224 R²¹ G²⁴ 1225 R²² G²¹ 1226 R²² G²² 1227 R²² G²³ 1228 R²² G²⁴ 1229 R²³ G²¹ 1230 R²³ G²² 1231 R²³ G²³ 1232 R²³ G²⁴ 1233 R²⁴ G²¹ 1234 R²⁴ G²² 1235 R²⁴ G²³ 1236 R²⁴ G²⁴ 1237 R²⁵ G²¹ 1238 R²⁵ G²² 1239 R²⁵ G²³ 1240 R²⁵ G²⁴ 1241 R²⁶ G²¹ 1242 R²⁶ G²² 1243 R²⁶ G²³ 1244 R²⁶ G²⁴ 1245 R²⁷ G²¹ 1246 R²⁷ G²² 1247 R²⁷ G²³ 1248 R²⁷ G²⁴ 1249 R²⁸ G²¹ 1250 R²⁸ G²² 1251 R²⁸ G²³ 1252 R²⁸ G²⁴ 1253 R²⁹ G²¹ 1254 R²⁹ G²² 1255 R²⁹ G²³ 1256 R²⁹ G²⁴ 1257 R³⁰ G²¹ 1258 R³⁰ G²² 1259 R³⁰ G²³ 1260 R³⁰ G²⁴ 1261 R³¹ G²¹ 1262 R³¹ G²² 1263 R³¹ G²³ 1264 R³¹ G²⁴ 1265 R³² G²¹ 1266 R³² G²² 1267 R³² G²³ 1268 R³² G²⁴ 1269 R³³ G²¹ 1270 R³³ G²² 1271 R³³ G²³ 1272 R³³ G²⁴ 1273 R³⁴ G²¹ 1274 R³⁴ G²² 1275 R³⁴ G²³ 1276 R³⁴ G²⁴ 1277 R³⁵ G²¹ 1278 R³⁵ G²² 1279 R³⁵ G²³ 1280 R³⁵ G²⁴ 1281 R³⁶ G²¹ 1282 R³⁶ G²² 1283 R³⁶ G²³ 1284 R³⁶ G²⁴ 1285 R³⁷ G²¹ 1286 R³⁷ G²² 1287 R³⁷ G²³ 1288 R³⁷ G²⁴ 1289 R³⁸ G²¹ 1290 R³⁸ G²² 1291 R³⁸ G²³ 1292 R³⁸ G²⁴ 1293 R³⁹ G²¹ 1294 R³⁹ G²² 1295 R³⁹ G²³ 1296 R³⁹ G²⁴ 1297 R⁴⁰ G²¹ 1298 R⁴⁰ G²² 1299 R⁴⁰ G²³ 1300 R⁴⁰ G²⁴ 1301 R⁴¹ G²¹ 1302 R⁴¹ G²² 1303 R⁴¹ G²³ 1304 R⁴¹ G²⁴ 1305 R⁴² G²¹ 1306 R⁴² G²² 1307 R⁴² G²³ 1308 R⁴² G²⁴ 1309 R⁴³ G²¹ 1310 R⁴³ G²² 1311 R⁴³ G²³ 1312 R⁴³ G²⁴ 1313 R⁴⁴ G²¹ 1314 R⁴⁴ G²² 1315 R⁴⁴ G²³ 1316 R⁴⁴ G²⁴ 1317 R⁴⁵ G²¹ 1318 R⁴⁵ G²² 1319 R⁴⁵ G²³ 1320 R⁴⁵ G²⁴ 1321 R⁴⁶ G²¹ 1322 R⁴⁶ G²² 1323 R⁴⁶ G²³ 1324 R⁴⁶ G²⁴ 1325 R⁴⁷ G²¹ 1326 R⁴⁷ G²² 1327 R⁴⁷ G²³ 1328 R⁴⁷ G²⁴ 1329 R⁴⁸ G²¹ 1330 R⁴⁸ G²² 1331 R⁴⁸ G²³ 1332 R⁴⁸ G²⁴ 1333 R⁴⁹ G²¹ 1334 R⁴⁹ G²² 1335 R⁴⁹ G²³ 1336 R⁴⁹ G²⁴ 1337 R⁵⁰ G²¹ 1338 R⁵⁰ G²² 1339 R⁵⁰ G²³ 1340 R⁵⁰ G²⁴ 1341 R⁵¹ G²¹ 1342 R⁵¹ G²² 1343 R⁵¹ G²³ 1344 R⁵¹ G²⁴ 1345 R⁵² G²¹ 1346 R⁵² G²² 1347 R⁵² G²³ 1348 R⁵² G²⁴ 1349 R⁵³ G²¹ 1350 R⁵³ G²² 1351 R⁵³ G²³ 1352 R⁵³ G²⁴ 1353 R⁵⁴ G²¹ 1354 R⁵⁴ G²² 1355 R⁵⁴ G²³ 1356 R⁵⁴ G²⁴ 1357 R⁵⁵ G²¹ 1358 R⁵⁵ G²² 1359 R⁵⁵ G²³ 1360 R⁵⁵ G²⁴ 1361 R⁵⁶ G²¹ 1362 R⁵⁶ G²² 1363 R⁵⁶ G²³ 1364 R⁵⁶ G²⁴ 1365 R⁵⁷ G²¹ 1366 R⁵⁷ G²² 1367 R⁵⁷ G²³ 1368 R⁵⁷ G²⁴ 1369 R¹ G²⁵ 1370 R¹ G²⁶ 1371 R¹ G²⁷ 1372 R¹ G²⁸ 1373 R² G²⁵ 1374 R² G²⁶ 1375 R² G²⁷ 1376 R² G²⁸ 1377 R³ G²⁵ 1378 R³ G²⁶ 1379 R³ G²⁷ 1380 R³ G²⁸ 1381 R⁴ G²⁵ 1382 R⁴ G²⁶ 1383 R⁴ G²⁷ 1384 R⁴ G²⁸ 1385 R⁵ G²⁵ 1386 R⁵ G²⁶ 1387 R⁵ G²⁷ 1388 R⁵ G²⁸ 1389 R⁶ G²⁵ 1390 R⁶ G²⁶ 1391 R⁶ G²⁷ 1392 R⁶ G²⁸ 1393 R⁷ G²⁵ 1394 R⁷ G²⁶ 1395 R⁷ G²⁷ 1396 R⁷ G²⁸ 1397 R⁸ G²⁵ 1398 R⁸ G²⁶ 1399 R⁸ G²⁷ 1400 R⁸ G²⁸ 1401 R⁹ G²⁵ 1402 R⁹ G²⁶ 1403 R⁹ G²⁷ 1404 R⁹ G²⁸ 1405 R¹⁰ G²⁵ 1406 R¹⁰ G²⁶ 1407 R¹⁰ G²⁷ 1408 R¹⁰ G²⁸ 1409 R¹¹ G²⁵ 1410 R¹¹ G²⁶ 1411 R¹¹ G²⁷ 1412 R¹¹ G²⁸ 1413 R¹² G²⁵ 1414 R¹² G²⁶ 1415 R¹² G²⁷ 1416 R¹² G²⁸ 1417 R¹³ G²⁵ 1418 R¹³ G²⁶ 1419 R¹³ G²⁷ 1420 R¹³ G²⁸ 1421 R¹⁴ G²⁵ 1422 R¹⁴ G²⁶ 1423 R¹⁴ G²⁷ 1424 R¹⁴ G²⁸ 1425 R¹⁵ G²⁵ 1426 R¹⁵ G²⁶ 1427 R¹⁵ G²⁷ 1428 R¹⁵ G²⁸ 1429 R¹⁶ G²⁵ 1430 R¹⁶ G²⁶ 1431 R¹⁶ G²⁷ 1432 R¹⁶ G²⁸ 1433 R¹⁷ G²⁵ 1434 R¹⁷ G²⁶ 1435 R¹⁷ G²⁷ 1436 R¹⁷ G²⁸ 1437 R¹⁸ G²⁵ 1438 R¹⁸ G²⁶ 1439 R¹⁸ G²⁷ 1440 R¹⁸ G²⁸ 1441 R¹⁹ G²⁵ 1442 R¹⁹ G²⁶ 1443 R¹⁹ G²⁷ 1444 R¹⁹ G²⁸ 1445 R²⁰ G²⁵ 1446 R²⁰ G²⁶ 1447 R²⁰ G²⁷ 1448 R²⁰ G²⁸ 1449 R²¹ G²⁵ 1450 R²¹ G²⁶ 1451 R²¹ G²⁷ 1452 R²¹ G²⁸ 1453 R²² G²⁵ 1454 R²² G²⁶ 1455 R²² G²⁷ 1456 R²² G²⁸ 1457 R²³ G²⁵ 1458 R²³ G²⁶ 1459 R²³ G²⁷ 1460 R²³ G²⁸ 1461 R²⁴ G²⁵ 1462 R²⁴ G²⁶ 1463 R²⁴ G²⁷ 1464 R²⁴ G²⁸ 1465 R²⁵ G²⁵ 1466 R²⁵ G²⁶ 1467 R²⁵ G²⁷ 1468 R²⁵ G²⁸ 1469 R²⁶ G²⁵ 1470 R²⁶ G²⁶ 1471 R²⁶ G²⁷ 1472 R²⁶ G²⁸ 1473 R²⁷ G²⁵ 1474 R²⁷ G²⁶ 1475 R²⁷ G²⁷ 1476 R²⁷ G²⁸ 1477 R²⁸ G²⁵ 1478 R²⁸ G²⁶ 1479 R²⁸ G²⁷ 1480 R²⁸ G²⁸ 1481 R²⁹ G²⁵ 1482 R²⁹ G²⁶ 1483 R²⁹ G²⁷ 1484 R²⁹ G²⁸ 1485 R³⁰ G²⁵ 1486 R³⁰ G²⁶ 1487 R³⁰ G²⁷ 1488 R³⁰ G²⁸ 1489 R³¹ G²⁵ 1490 R³¹ G²⁶ 1491 R³¹ G²⁷ 1492 R³¹ G²⁸ 1493 R³² G²⁵ 1494 R³² G²⁶ 1495 R³² G²⁷ 1496 R³² G²⁸ 1497 R³³ G²⁵ 1498 R³³ G²⁶ 1499 R³³ G²⁷ 1500 R³³ G²⁸ 1501 R³⁴ G²⁵ 1502 R³⁴ G²⁶ 1503 R³⁴ G²⁷ 1504 R³⁴ G²⁸ 1505 R³⁵ G²⁵ 1506 R³⁵ G²⁶ 1507 R³⁵ G²⁷ 1508 R³⁵ G²⁸ 1509 R³⁶ G²⁵ 1510 R³⁶ G²⁶ 1511 R³⁶ G²⁷ 1512 R³⁶ G²⁸ 1513 R³⁷ G²⁵ 1514 R³⁷ G²⁶ 1515 R³⁷ G²⁷ 1516 R³⁷ G²⁸ 1517 R³⁸ G²⁵ 1518 R³⁸ G²⁶ 1519 R³⁸ G²⁷ 1520 R³⁸ G²⁸ 1521 R³⁹ G²⁵ 1522 R³⁹ G²⁶ 1523 R³⁹ G²⁷ 1524 R³⁹ G²⁸ 1525 R⁴⁰ G²⁵ 1526 R⁴⁰ G²⁶ 1527 R⁴⁰ G²⁷ 1528 R⁴⁰ G²⁸ 1529 R⁴¹ G²⁵ 1530 R⁴¹ G²⁶ 1531 R⁴¹ G²⁷ 1532 R⁴¹ G²⁸ 1533 R⁴² G²⁵ 1534 R⁴² G²⁶ 1535 R⁴² G²⁷ 1536 R⁴² G²⁸ 1537 R⁴³ G²⁵ 1538 R⁴³ G²⁶ 1539 R⁴³ G²⁷ 1540 R⁴³ G²⁸ 1541 R⁴⁴ G²⁵ 1542 R⁴⁴ G²⁶ 1543 R⁴⁴ G²⁷ 1544 R⁴⁴ G²⁸ 1545 R⁴⁵ G²⁵ 1546 R⁴⁵ G²⁶ 1547 R⁴⁵ G²⁷ 1548 R⁴⁵ G²⁸ 1549 R⁴⁶ G²⁵ 1550 R⁴⁶ G²⁶ 1551 R⁴⁶ G²⁷ 1552 R⁴⁶ G²⁸ 1553 R⁴⁷ G²⁵ 1554 R⁴⁷ G²⁶ 1555 R⁴⁷ G²⁷ 1556 R⁴⁷ G²⁸ 1557 R⁴⁸ G²⁵ 1558 R⁴⁸ G²⁶ 1559 R⁴⁸ G²⁷ 1560 R⁴⁸ G²⁸ 1561 R⁴⁹ G²⁵ 1562 R⁴⁹ G²⁶ 1563 R⁴⁹ G²⁷ 1564 R⁴⁹ G²⁸ 1565 R⁵⁰ G²⁵ 1566 R⁵⁰ G²⁶ 1567 R⁵⁰ G²⁷ 1568 R⁵⁰ G²⁸ 1569 R⁵¹ G²⁵ 1570 R⁵¹ G²⁶ 1571 R⁵¹ G²⁷ 1572 R⁵¹ G²⁸ 1573 R⁵² G²⁵ 1574 R⁵² G²⁶ 1575 R⁵² G²⁷ 1576 R⁵² G²⁸ 1577 R⁵³ G²⁵ 1578 R⁵³ G²⁶ 1579 R⁵³ G²⁷ 1580 R⁵³ G²⁸ 1581 R⁵⁴ G²⁵ 1582 R⁵⁴ G²⁶ 1583 R⁵⁴ G²⁷ 1584 R⁵⁴ G²⁸ 1585 R⁵⁵ G²⁵ 1586 R⁵⁵ G²⁶ 1587 R⁵⁵ G²⁷ 1588 R⁵⁵ G²⁸ 1589 R⁵⁶ G²⁵ 1590 R⁵⁶ G²⁶ 1591 R⁵⁶ G²⁷ 1592 R⁵⁶ G²⁸ 1593 R⁵⁷ G²⁵ 1594 R⁵⁷ G²⁶ 1595 R⁵⁷ G²⁷ 1596 R⁵⁷ G²⁸ 1597 R¹ G²⁹ 1598 R¹ G³⁰ 1599 R¹ G³¹ 1600 R¹ G³² 1601 R² G²⁹ 1602 R² G³⁰ 1603 R² G³¹ 1604 R² G³² 1605 R³ G²⁹ 1606 R³ G³⁰ 1607 R³ G³¹ 1608 R³ G³² 1609 R⁴ G²⁹ 1610 R⁴ G³⁰ 1611 R⁴ G³¹ 1612 R⁴ G³² 1613 R⁵ G²⁹ 1614 R⁵ G³⁰ 1615 R⁵ G³¹ 1616 R⁵ G³² 1617 R⁶ G²⁹ 1618 R⁶ G³⁰ 1619 R⁶ G³¹ 1620 R⁶ G³² 1621 R⁷ G²⁹ 1622 R⁷ G³⁰ 1623 R⁷ G³¹ 1624 R⁷ G³² 1625 R⁸ G²⁹ 1626 R⁸ G³⁰ 1627 R⁸ G³¹ 1628 R⁸ G³² 1629 R⁹ G²⁹ 1630 R⁹ G³⁰ 1631 R⁹ G³¹ 1632 R⁹ G³² 1633 R¹⁰ G²⁹ 1634 R¹⁰ G³⁰ 1635 R¹⁰ G³¹ 1636 R¹⁰ G³² 1637 R¹¹ G²⁹ 1638 R¹¹ G³⁰ 1639 R¹¹ G³¹ 1640 R¹¹ G³² 1641 R¹² G²⁹ 1642 R¹² G³⁰ 1643 R¹² G³¹ 1644 R¹² G³² 1645 R¹³ G²⁹ 1646 R¹³ G³⁰ 1647 R¹³ G³¹ 1648 R¹³ G³² 1649 R¹⁴ G²⁹ 1650 R¹⁴ G³⁰ 1651 R¹⁴ G³¹ 1652 R¹⁴ G³² 1653 R¹⁵ G²⁹ 1654 R¹⁵ G³⁰ 1655 R¹⁵ G³¹ 1656 R¹⁵ G³² 1657 R¹⁶ G²⁹ 1658 R¹⁶ G³⁰ 1659 R¹⁶ G³¹ 1660 R¹⁶ G³² 1661 R¹⁷ G²⁹ 1662 R¹⁷ G³⁰ 1663 R¹⁷ G³¹ 1664 R¹⁷ G³² 1665 R¹⁸ G²⁹ 1666 R¹⁸ G³⁰ 1667 R¹⁸ G³¹ 1668 R¹⁸ G³² 1669 R¹⁹ G²⁹ 1670 R¹⁹ G³⁰ 1671 R¹⁹ G³¹ 1672 R¹⁹ G³² 1673 R²⁰ G²⁹ 1674 R²⁰ G³⁰ 1675 R²⁰ G³¹ 1676 R²⁰ G³² 1677 R²¹ G²⁹ 1678 R²¹ G³⁰ 1679 R²¹ G³¹ 1680 R²¹ G³² 1681 R²² G²⁹ 1682 R²² G³⁰ 1683 R²² G³¹ 1684 R²² G³² 1685 R²³ G²⁹ 1686 R²³ G³⁰ 1687 R²³ G³¹ 1688 R²³ G³² 1689 R²⁴ G²⁹ 1690 R²⁴ G³⁰ 1691 R²⁴ G³¹ 1692 R²⁴ G³² 1693 R²⁵ G²⁹ 1694 R²⁵ G³⁰ 1695 R²⁵ G³¹ 1696 R²⁵ G³² 1697 R²⁶ G²⁹ 1698 R²⁶ G³⁰ 1699 R²⁶ G³¹ 1700 R²⁶ G³² 1701 R²⁷ G²⁹ 1702 R²⁷ G³⁰ 1703 R²⁷ G³¹ 1704 R²⁷ G³² 1705 R²⁸ G²⁹ 1706 R²⁸ G³⁰ 1707 R²⁸ G³¹ 1708 R²⁸ G³² 1709 R²⁹ G²⁹ 1710 R²⁹ G³⁰ 1711 R²⁹ G³¹ 1712 R²⁹ G³² 1713 R³⁰ G²⁹ 1714 R³⁰ G³⁰ 1715 R³⁰ G³¹ 1716 R³⁰ G³² 1717 R³¹ G²⁹ 1718 R³¹ G³⁰ 1719 R³¹ G³¹ 1720 R³¹ G³² 1721 R³² G²⁹ 1722 R³² G³⁰ 1723 R³² G³¹ 1724 R³² G³² 1725 R³³ G²⁹ 1726 R³³ G³⁰ 1727 R³³ G³¹ 1728 R³³ G³² 1729 R³⁴ G²⁹ 1730 R³⁴ G³⁰ 1731 R³⁴ G³¹ 1732 R³⁴ G³² 1733 R³⁵ G²⁹ 1734 R³⁵ G³⁰ 1735 R³⁵ G³¹ 1736 R³⁵ G³² 1737 R³⁶ G²⁹ 1738 R³⁶ G³⁰ 1739 R³⁶ G³¹ 1740 R³⁶ G³² 1741 R³⁷ G²⁹ 1742 R³⁷ G³⁰ 1743 R³⁷ G³¹ 1744 R³⁷ G³² 1745 R³⁸ G²⁹ 1746 R³⁸ G³⁰ 1747 R³⁸ G³¹ 1748 R³⁸ G³² 1749 R³⁹ G²⁹ 1750 R³⁹ G³⁰ 1751 R³⁹ G³¹ 1752 R³⁹ G³² 1753 R⁴⁰ G²⁹ 1754 R⁴⁰ G³⁰ 1755 R⁴⁰ G³¹ 1756 R⁴⁰ G³² 1757 R⁴¹ G²⁹ 1758 R⁴¹ G³⁰ 1759 R⁴¹ G³¹ 1760 R⁴¹ G³² 1761 R⁴² G²⁹ 1762 R⁴² G³⁰ 1763 R⁴² G³¹ 1764 R⁴² G³² 1765 R⁴³ G²⁹ 1766 R⁴³ G³⁰ 1767 R⁴³ G³¹ 1768 R⁴³ G³² 1769 R⁴⁴ G²⁹ 1770 R⁴⁴ G³⁰ 1771 R⁴⁴ G³¹ 1772 R⁴⁴ G³² 1773 R⁴⁵ G²⁹ 1774 R⁴⁵ G³⁰ 1775 R⁴⁵ G³¹ 1776 R⁴⁵ G³² 1777 R⁴⁶ G²⁹ 1778 R⁴⁶ G³⁰ 1779 R⁴⁶ G³¹ 1780 R⁴⁶ G³² 1781 R⁴⁷ G²⁹ 1782 R⁴⁷ G³⁰ 1783 R⁴⁷ G³¹ 1784 R⁴⁷ G³² 1785 R⁴⁸ G²⁹ 1786 R⁴⁸ G³⁰ 1787 R⁴⁸ G³¹ 1788 R⁴⁸ G³² 1789 R⁴⁹ G²⁹ 1790 R⁴⁹ G³⁰ 1791 R⁴⁹ G³¹ 1792 R⁴⁹ G³² 1793 R⁵⁰ G²⁹ 1794 R⁵⁰ G³⁰ 1795 R⁵⁰ G³¹ 1796 R⁵⁰ G³² 1797 R⁵¹ G²⁹ 1798 R⁵¹ G³⁰ 1799 R⁵¹ G³¹ 1800 R⁵¹ G³² 1801 R⁵² G²⁹ 1802 R⁵² G³⁰ 1803 R⁵² G³¹ 1804 R⁵² G³² 1805 R⁵³ G²⁹ 1806 R⁵³ G³⁰ 1807 R⁵³ G³¹ 1808 R⁵³ G³² 1809 R⁵⁴ G²⁹ 1810 R⁵⁴ G³⁰ 1811 R⁵⁴ G³¹ 1812 R⁵⁴ G³² 1813 R⁵⁵ G²⁹ 1814 R⁵⁵ G³⁰ 1815 R⁵⁵ G³¹ 1816 R⁵⁵ G³² 1817 R⁵⁶ G²⁹ 1818 R⁵⁶ G³⁰ 1819 R⁵⁶ G³¹ 1820 R⁵⁶ G³² 1821 R⁵⁷ G²⁹ 1822 R⁵⁷ G³⁰ 1823 R⁵⁷ G³¹ 1824 R⁵⁷ G³² 1825 R¹ G³³ 1826 R¹ G³⁴ 1827 R¹ G³⁵ 1828 R¹ G³⁶ 1829 R² G³³ 1830 R² G³⁴ 1831 R² G³⁵ 1832 R² G³⁶ 1833 R³ G³³ 1834 R³ G³⁴ 1835 R³ G³⁵ 1836 R³ G³⁶ 1837 R⁴ G³³ 1838 R⁴ G³⁴ 1839 R⁴ G³⁵ 1840 R⁴ G³⁶ 1841 R⁵ G³³ 1842 R⁵ G³⁴ 1843 R⁵ G³⁵ 1844 R⁵ G³⁶ 1845 R⁶ G³³ 1846 R⁶ G³⁴ 1847 R⁶ G³⁵ 1848 R⁶ G³⁶ 1849 R⁷ G³³ 1850 R⁷ G³⁴ 1851 R⁷ G³⁵ 1852 R⁷ G³⁶ 1853 R⁸ G³³ 1854 R⁸ G³⁴ 1855 R⁸ G³⁵ 1856 R⁸ G³⁶ 1857 R⁹ G³³ 1858 R⁹ G³⁴ 1859 R⁹ G³⁵ 1860 R⁹ G³⁶ 1861 R¹⁰ G³³ 1862 R¹⁰ G³⁴ 1863 R¹⁰ G³⁵ 1864 R¹⁰ G³⁶ 1865 R¹¹ G³³ 1866 R¹¹ G³⁴ 1867 R¹¹ G³⁵ 1868 R¹¹ G³⁶ 1869 R¹² G³³ 1870 R¹² G³⁴ 1871 R¹² G³⁵ 1872 R¹² G³⁶ 1873 R¹³ G³³ 1874 R¹³ G³⁴ 1875 R¹³ G³⁵ 1876 R¹³ G³⁶ 1877 R¹⁴ G³³ 1878 R¹⁴ G³⁴ 1879 R¹⁴ G³⁵ 1880 R¹⁴ G³⁶ 1881 R¹⁵ G³³ 1882 R¹⁵ G³⁴ 1883 R¹⁵ G³⁵ 1884 R¹⁵ G³⁶ 1885 R¹⁶ G³³ 1886 R¹⁶ G³⁴ 1887 R¹⁶ G³⁵ 1888 R¹⁶ G³⁶ 1889 R¹⁷ G³³ 1890 R¹⁷ G³⁴ 1891 R¹⁷ G³⁵ 1892 R¹⁷ G³⁶ 1893 R¹⁸ G³³ 1894 R¹⁸ G³⁴ 1895 R¹⁸ G³⁵ 1896 R¹⁸ G³⁶ 1897 R¹⁹ G³³ 1898 R¹⁹ G³⁴ 1899 R¹⁹ G³⁵ 1900 R¹⁹ G³⁶ 1901 R²⁰ G³³ 1902 R²⁰ G³⁴ 1903 R²⁰ G³⁵ 1904 R²⁰ G³⁶ 1905 R²¹ G³³ 1906 R²¹ G³⁴ 1907 R²¹ G³⁵ 1908 R²¹ G³⁶ 1909 R²² G³³ 1910 R²² G³⁴ 1911 R²² G³⁵ 1912 R²² G³⁶ 1913 R²³ G³³ 1914 R²³ G³⁴ 1915 R²³ G³⁵ 1916 R²³ G³⁶ 1917 R²⁴ G³³ 1918 R²⁴ G³⁴ 1919 R²⁴ G³⁵ 1920 R²⁴ G³⁶ 1921 R²⁵ G³³ 1922 R²⁵ G³⁴ 1923 R²⁵ G³⁵ 1924 R²⁵ G³⁶ 1925 R²⁶ G³³ 1926 R²⁶ G³⁴ 1927 R²⁶ G³⁵ 1928 R²⁶ G³⁶ 1929 R²⁷ G³³ 1930 R²⁷ G³⁴ 1931 R²⁷ G³⁵ 1932 R²⁷ G³⁶ 1933 R²⁸ G³³ 1934 R²⁸ G³⁴ 1935 R²⁸ G³⁵ 1936 R²⁸ G³⁶ 1937 R²⁹ G³³ 1938 R²⁹ G³⁴ 1939 R²⁹ G³⁵ 1940 R²⁹ G³⁶ 1941 R³⁰ G³³ 1942 R³⁰ G³⁴ 1943 R³⁰ G³⁵ 1944 R³⁰ G³⁶ 1945 R³¹ G³³ 1946 R³¹ G³⁴ 1947 R³¹ G³⁵ 1948 R³¹ G³⁶ 1949 R³² G³³ 1950 R³² G³⁴ 1951 R³² G³⁵ 1952 R³² G³⁶ 1953 R³³ G³³ 1954 R³³ G³⁴ 1955 R³³ G³⁵ 1956 R³³ G³⁶ 1957 R³⁴ G³³ 1958 R³⁴ G³⁴ 1959 R³⁴ G³⁵ 1960 R³⁴ G³⁶ 1961 R³⁵ G³³ 1962 R³⁵ G³⁴ 1963 R³⁵ G³⁵ 1964 R³⁵ G³⁶ 1965 R³⁶ G³³ 1966 R³⁶ G³⁴ 1967 R³⁶ G³⁵ 1968 R³⁶ G³⁶ 1969 R³⁷ G³³ 1970 R³⁷ G³⁴ 1971 R³⁷ G³⁵ 1972 R³⁷ G³⁶ 1973 R³⁸ G³³ 1974 R³⁸ G³⁴ 1975 R³⁸ G³⁵ 1976 R³⁸ G³⁶ 1977 R³⁹ G³³ 1978 R³⁹ G³⁴ 1979 R³⁹ G³⁵ 1980 R³⁹ G³⁶ 1981 R⁴⁰ G³³ 1982 R⁴⁰ G³⁴ 1983 R⁴⁰ G³⁵ 1984 R⁴⁰ G³⁶ 1985 R⁴¹ G³³ 1986 R⁴¹ G³⁴ 1987 R⁴¹ G³⁵ 1988 R⁴¹ G³⁶ 1989 R⁴² G³³ 1990 R⁴² G³⁴ 1991 R⁴² G³⁵ 1992 R⁴² G³⁶ 1993 R⁴³ G³³ 1994 R⁴³ G³⁴ 1995 R⁴³ G³⁵ 1996 R⁴³ G³⁶ 1997 R⁴⁴ G³³ 1998 R⁴⁴ G³⁴ 1999 R⁴⁴ G³⁵ 2000 R⁴⁴ G³⁶ 2001 R⁴⁵ G³³ 2002 R⁴⁵ G³⁴ 2003 R⁴⁵ G³⁵ 2004 R⁴⁵ G³⁶ 2005 R⁴⁶ G³³ 2006 R⁴⁶ G³⁴ 2007 R⁴⁶ G³⁵ 2008 R⁴⁶ G³⁶ 2009 R⁴⁷ G³³ 2010 R⁴⁷ G³⁴ 2011 R⁴⁷ G³⁵ 2012 R⁴⁷ G³⁶ 2013 R⁴⁸ G³³ 2014 R⁴⁸ G³⁴ 2015 R⁴⁸ G³⁵ 2016 R⁴⁸ G³⁶ 2017 R⁴⁹ G³³ 2018 R⁴⁹ G³⁴ 2019 R⁴⁹ G³⁵ 2020 R⁴⁹ G³⁶ 2021 R⁵⁰ G³³ 2022 R⁵⁰ G³⁴ 2023 R⁵⁰ G³⁵ 2024 R⁵⁰ G³⁶ 2025 R⁵¹ G³³ 2026 R⁵¹ G³⁴ 2027 R⁵¹ G³⁵ 2028 R⁵¹ G³⁶ 2029 R⁵² G³³ 2030 R⁵² G³⁴ 2031 R⁵² G³⁵ 2032 R⁵² G³⁶ 2033 R⁵³ G³³ 2034 R⁵³ G³⁴ 2035 R⁵³ G³⁵ 2036 R⁵³ G³⁶ 2037 R⁵⁴ G³³ 2038 R⁵⁴ G³⁴ 2039 R⁵⁴ G³⁵ 2040 R⁵⁴ G³⁶ 2041 R⁵⁵ G³³ 2042 R⁵⁵ G³⁴ 2043 R⁵⁵ G³⁵ 2044 R⁵⁵ G³⁶ 2045 R⁵⁶ G³³ 2046 R⁵⁶ G³⁴ 2047 R⁵⁶ G³⁵ 2048 R⁵⁶ G³⁶ 2049 R⁵⁷ G³³ 2050 R⁵⁷ G³⁴ 2051 R⁵⁷ G³⁵ 2052 R⁵⁷ G³⁶ 2053 R¹ G³⁷ 2054 R¹ G³⁸ 2055 R¹ G³⁹ 2056 R¹ G⁴⁰ 2057 R² G³⁷ 2058 R² G³⁸ 2059 R² G³⁹ 2060 R² G⁴⁰ 2061 R³ G³⁷ 2062 R³ G³⁸ 2063 R³ G³⁹ 2064 R³ G⁴⁰ 2065 R⁴ G³⁷ 2066 R⁴ G³⁸ 2067 R⁴ G³⁹ 2068 R⁴ G⁴⁰ 2069 R⁵ G³⁷ 2070 R⁵ G³⁸ 2071 R⁵ G³⁹ 2072 R⁵ G⁴⁰ 2073 R⁶ G³⁷ 2074 R⁶ G³⁸ 2075 R⁶ G³⁹ 2076 R⁶ G⁴⁰ 2077 R⁷ G³⁷ 2078 R⁷ G³⁸ 2079 R⁷ G³⁹ 2080 R⁷ G⁴⁰ 2081 R⁸ G³⁷ 2082 R⁸ G³⁸ 2083 R⁸ G³⁹ 2084 R⁸ G⁴⁰ 2085 R⁹ G³⁷ 2086 R⁹ G³⁸ 2087 R⁹ G³⁹ 2088 R⁹ G⁴⁰ 2089 R¹⁰ G³⁷ 2090 R¹⁰ G³⁸ 2091 R¹⁰ G³⁹ 2092 R¹⁰ G⁴⁰ 2093 R¹¹ G³⁷ 2094 R¹¹ G³⁸ 2095 R¹¹ G³⁹ 2096 R¹¹ G⁴⁰ 2097 R¹² G³⁷ 2098 R¹² G³⁸ 2099 R¹² G³⁹ 2100 R¹² G⁴⁰ 2101 R¹³ G³⁷ 2102 R¹³ G³⁸ 2103 R¹³ G³⁹ 2104 R¹³ G⁴⁰ 2105 R¹⁴ G³⁷ 2106 R¹⁴ G³⁸ 2107 R¹⁴ G³⁹ 2108 R¹⁴ G⁴⁰ 2109 R¹⁵ G³⁷ 2110 R¹⁵ G³⁸ 2111 R¹⁵ G³⁹ 2112 R¹⁵ G⁴⁰ 2113 R¹⁶ G³⁷ 2114 R¹⁶ G³⁸ 2115 R¹⁶ G³⁹ 2116 R¹⁶ G⁴⁰ 2117 R¹⁷ G³⁷ 2118 R¹⁷ G³⁸ 2119 R¹⁷ G³⁹ 2120 R¹⁷ G⁴⁰ 2121 R¹⁸ G³⁷ 2122 R¹⁸ G³⁸ 2123 R¹⁸ G³⁹ 2124 R¹⁸ G⁴⁰ 2125 R¹⁹ G³⁷ 2126 R¹⁹ G³⁸ 2127 R¹⁹ G³⁹ 2128 R¹⁹ G⁴⁰ 2129 R²⁰ G³⁷ 2130 R²⁰ G³⁸ 2131 R²⁰ G³⁹ 2132 R²⁰ G⁴⁰ 2133 R²¹ G³⁷ 2134 R²¹ G³⁸ 2135 R²¹ G³⁹ 2136 R²¹ G⁴⁰ 2137 R²² G³⁷ 2138 R²² G³⁸ 2139 R²² G³⁹ 2140 R²² G⁴⁰ 2141 R²³ G³⁷ 2142 R²³ G³⁸ 2143 R²³ G³⁹ 2144 R²³ G⁴⁰ 2145 R²⁴ G³⁷ 2146 R²⁴ G³⁸ 2147 R²⁴ G³⁹ 2148 R²⁴ G⁴⁰ 2149 R²⁵ G³⁷ 2150 R²⁵ G³⁸ 2151 R²⁵ G³⁹ 2152 R²⁵ G⁴⁰ 2153 R²⁶ G³⁷ 2154 R²⁶ G³⁸ 2155 R²⁶ G³⁹ 2156 R²⁶ G⁴⁰ 2157 R²⁷ G³⁷ 2158 R²⁷ G³⁸ 2159 R²⁷ G³⁹ 2160 R²⁷ G⁴⁰ 2161 R²⁸ G³⁷ 2162 R²⁸ G³⁸ 2163 R²⁸ G³⁹ 2164 R²⁸ G⁴⁰ 2165 R²⁹ G³⁷ 2166 R²⁹ G³⁸ 2167 R²⁹ G³⁹ 2168 R²⁹ G⁴⁰ 2169 R³⁰ G³⁷ 2170 R³⁰ G³⁸ 2171 R³⁰ G³⁹ 2172 R³⁰ G⁴⁰ 2173 R³¹ G³⁷ 2174 R³¹ G³⁸ 2175 R³¹ G³⁹ 2176 R³¹ G⁴⁰ 2177 R³² G³⁷ 2178 R³² G³⁸ 2179 R³² G³⁹ 2180 R³² G⁴⁰ 2181 R³³ G³⁷ 2182 R³³ G³⁸ 2183 R³³ G³⁹ 2184 R³³ G⁴⁰ 2185 R³⁴ G³⁷ 2186 R³⁴ G³⁸ 2187 R³⁴ G³⁹ 2188 R³⁴ G⁴⁰ 2189 R³⁵ G³⁷ 2190 R³⁵ G³⁸ 2191 R³⁵ G³⁹ 2192 R³⁵ G⁴⁰ 2193 R³⁶ G³⁷ 2194 R³⁶ G³⁸ 2195 R³⁶ G³⁹ 2196 R³⁶ G⁴⁰ 2197 R³⁷ G³⁷ 2198 R³⁷ G³⁸ 2199 R³⁷ G³⁹ 2200 R³⁷ G⁴⁰ 2201 R³⁸ G³⁷ 2202 R³⁸ G³⁸ 2203 R³⁸ G³⁹ 2204 R³⁸ G⁴⁰ 2205 R³⁹ G³⁷ 2206 R³⁹ G³⁸ 2207 R³⁹ G³⁹ 2208 R³⁹ G⁴⁰ 2209 R⁴⁰ G³⁷ 2210 R⁴⁰ G³⁸ 2211 R⁴⁰ G³⁹ 2212 R⁴⁰ G⁴⁰ 2213 R⁴¹ G³⁷ 2214 R⁴¹ G³⁸ 2215 R⁴¹ G³⁹ 2216 R⁴¹ G⁴⁰ 2217 R⁴² G³⁷ 2218 R⁴² G³⁸ 2219 R⁴² G³⁹ 2220 R⁴² G⁴⁰ 2221 R⁴³ G³⁷ 2222 R⁴³ G³⁸ 2223 R⁴³ G³⁹ 2224 R⁴³ G⁴⁰ 2225 R⁴⁴ G³⁷ 2226 R⁴⁴ G³⁸ 2227 R⁴⁴ G³⁹ 2228 R⁴⁴ G⁴⁰ 2229 R⁴⁵ G³⁷ 2230 R⁴⁵ G³⁸ 2231 R⁴⁵ G³⁹ 2232 R⁴⁵ G⁴⁰ 2233 R⁴⁶ G³⁷ 2234 R⁴⁶ G³⁸ 2235 R⁴⁶ G³⁹ 2236 R⁴⁶ G⁴⁰ 2237 R⁴⁷ G³⁷ 2238 R⁴⁷ G³⁸ 2239 R⁴⁷ G³⁹ 2240 R⁴⁷ G⁴⁰ 2241 R⁴⁸ G³⁷ 2242 R⁴⁸ G³⁸ 2243 R⁴⁸ G³⁹ 2244 R⁴⁸ G⁴⁰ 2245 R⁴⁹ G³⁷ 2246 R⁴⁹ G³⁸ 2247 R⁴⁹ G³⁹ 2248 R⁴⁹ G⁴⁰ 2249 R⁵⁰ G³⁷ 2250 R⁵⁰ G³⁸ 2251 R⁵⁰ G³⁹ 2252 R⁵⁰ G⁴⁰ 2253 R⁵¹ G³⁷ 2254 R⁵¹ G³⁸ 2255 R⁵¹ G³⁹ 2256 R⁵¹ G⁴⁰ 2257 R⁵² G³⁷ 2258 R⁵² G³⁸ 2259 R⁵² G³⁹ 2260 R⁵² G⁴⁰ 2261 R⁵³ G³⁷ 2262 R⁵³ G³⁸ 2263 R⁵³ G³⁹ 2264 R⁵³ G⁴⁰ 2265 R⁵⁴ G³⁷ 2266 R⁵⁴ G³⁸ 2267 R⁵⁴ G³⁹ 2268 R⁵⁴ G⁴⁰ 2269 R⁵⁵ G³⁷ 2270 R⁵⁵ G³⁸ 2271 R⁵⁵ G³⁹ 2272 R⁵⁵ G⁴⁰ 2273 R⁵⁶ G³⁷ 2274 R⁵⁶ G³⁸ 2275 R⁵⁶ G³⁹ 2276 R⁵⁶ G⁴⁰ 2277 R⁵⁷ G³⁷ 2278 R⁵⁷ G³⁸ 2279 R⁵⁷ G³⁹ 2280 R⁵⁷ G⁴⁰ 2281 R¹ G⁴¹ 2282 R¹ G⁴² 2283 R¹ G⁴³ 2284 R¹ G⁴⁴ 2285 R² G⁴¹ 2286 R² G⁴² 2287 R² G⁴³ 2288 R² G⁴⁴ 2289 R³ G⁴¹ 2290 R³ G⁴² 2291 R³ G⁴³ 2292 R³ G⁴⁴ 2293 R⁴ G⁴¹ 2294 R⁴ G⁴² 2295 R⁴ G⁴³ 2296 R⁴ G⁴⁴ 2297 R⁵ G⁴¹ 2298 R⁵ G⁴² 2299 R⁵ G⁴³ 2300 R⁵ G⁴⁴ 2301 R⁶ G⁴¹ 2302 R⁶ G⁴² 2303 R⁶ G⁴³ 2304 R⁶ G⁴⁴ 2305 R⁷ G⁴¹ 2306 R⁷ G⁴² 2307 R⁷ G⁴³ 2308 R⁷ G⁴⁴ 2309 R⁸ G⁴¹ 2310 R⁸ G⁴² 2311 R⁸ G⁴³ 2312 R⁸ G⁴⁴ 2313 R⁹ G⁴¹ 2314 R⁹ G⁴² 2315 R⁹ G⁴³ 2316 R⁹ G⁴⁴ 2317 R¹⁰ G⁴¹ 2318 R¹⁰ G⁴² 2319 R¹⁰ G⁴³ 2320 R¹⁰ G⁴⁴ 2321 R¹¹ G⁴¹ 2322 R¹¹ G⁴² 2323 R¹¹ G⁴³ 2324 R¹¹ G⁴⁴ 2325 R¹² G⁴¹ 2326 R¹² G⁴² 2327 R¹² G⁴³ 2328 R¹² G⁴⁴ 2329 R¹³ G⁴¹ 2330 R¹³ G⁴² 2331 R¹³ G⁴³ 2332 R¹³ G⁴⁴ 2333 R¹⁴ G⁴¹ 2334 R¹⁴ G⁴² 2335 R¹⁴ G⁴³ 2336 R¹⁴ G⁴⁴ 2337 R¹⁵ G⁴¹ 2338 R¹⁵ G⁴² 2339 R¹⁵ G⁴³ 2340 R¹⁵ G⁴⁴ 2341 R¹⁶ G⁴¹ 2342 R¹⁶ G⁴² 2343 R¹⁶ G⁴³ 2344 R¹⁶ G⁴⁴ 2345 R¹⁷ G⁴¹ 2346 R¹⁷ G⁴² 2347 R¹⁷ G⁴³ 2348 R¹⁷ G⁴⁴ 2349 R¹⁸ G⁴¹ 2350 R¹⁸ G⁴² 2351 R¹⁸ G⁴³ 2352 R¹⁸ G⁴⁴ 2353 R¹⁹ G⁴¹ 2354 R¹⁹ G⁴² 2355 R¹⁹ G⁴³ 2356 R¹⁹ G⁴⁴ 2357 R²⁰ G⁴¹ 2358 R²⁰ G⁴² 2359 R²⁰ G⁴³ 2360 R²⁰ G⁴⁴ 2361 R²¹ G⁴¹ 2362 R²¹ G⁴² 2363 R²¹ G⁴³ 2364 R²¹ G⁴⁴ 2365 R²² G⁴¹ 2366 R²² G⁴² 2367 R²² G⁴³ 2368 R²² G⁴⁴ 2369 R²³ G⁴¹ 2370 R²³ G⁴² 2371 R²³ G⁴³ 2372 R²³ G⁴⁴ 2373 R²⁴ G⁴¹ 2374 R²⁴ G⁴² 2375 R²⁴ G⁴³ 2376 R²⁴ G⁴⁴ 2377 R²⁵ G⁴¹ 2378 R²⁵ G⁴² 2379 R²⁵ G⁴³ 2380 R²⁵ G⁴⁴ 2381 R²⁶ G⁴¹ 2382 R²⁶ G⁴² 2383 R²⁶ G⁴³ 2384 R²⁶ G⁴⁴ 2385 R²⁷ G⁴¹ 2386 R²⁷ G⁴² 2387 R²⁷ G⁴³ 2388 R²⁷ G⁴⁴ 2389 R²⁸ G⁴¹ 2390 R²⁸ G⁴² 2391 R²⁸ G⁴³ 2392 R²⁸ G⁴⁴ 2393 R²⁹ G⁴¹ 2394 R²⁹ G⁴² 2395 R²⁹ G⁴³ 2396 R²⁹ G⁴⁴ 2397 R³⁰ G⁴¹ 2398 R³⁰ G⁴² 2399 R³⁰ G⁴³ 2400 R³⁰ G⁴⁴ 2401 R³¹ G⁴¹ 2402 R³¹ G⁴² 2403 R³¹ G⁴³ 2404 R³¹ G⁴⁴ 2405 R³² G⁴¹ 2406 R³² G⁴² 2407 R³² G⁴³ 2408 R³² G⁴⁴ 2409 R³³ G⁴¹ 2410 R³³ G⁴² 2411 R³³ G⁴³ 2412 R³³ G⁴⁴ 2413 R³⁴ G⁴¹ 2414 R³⁴ G⁴² 2415 R³⁴ G⁴³ 2416 R³⁴ G⁴⁴ 2417 R³⁵ G⁴¹ 2418 R³⁵ G⁴² 2419 R³⁵ G⁴³ 2420 R³⁵ G⁴⁴ 2421 R³⁶ G⁴¹ 2422 R³⁶ G⁴² 2423 R³⁶ G⁴³ 2424 R³⁶ G⁴⁴ 2425 R³⁷ G⁴¹ 2426 R³⁷ G⁴² 2427 R³⁷ G⁴³ 2428 R³⁷ G⁴⁴ 2429 R³⁸ G⁴¹ 2430 R³⁸ G⁴² 2431 R³⁸ G⁴³ 2432 R³⁸ G⁴⁴ 2433 R³⁹ G⁴¹ 2434 R³⁹ G⁴² 2435 R³⁹ G⁴³ 2436 R³⁹ G⁴⁴ 2437 R⁴⁰ G⁴¹ 2438 R⁴⁰ G⁴² 2439 R⁴⁰ G⁴³ 2440 R⁴⁰ G⁴⁴ 2441 R⁴¹ G⁴¹ 2442 R⁴¹ G⁴² 2443 R⁴¹ G⁴³ 2444 R⁴¹ G⁴⁴ 2445 R⁴² G⁴¹ 2446 R⁴² G⁴² 2447 R⁴² G⁴³ 2448 R⁴² G⁴⁴ 2449 R⁴³ G⁴¹ 2450 R⁴³ G⁴² 2451 R⁴³ G⁴³ 2452 R⁴³ G⁴⁴ 2453 R⁴⁴ G⁴¹ 2454 R⁴⁴ G⁴² 2455 R⁴⁴ G⁴³ 2456 R⁴⁴ G⁴⁴ 2457 R⁴⁵ G⁴¹ 2458 R⁴⁵ G⁴² 2459 R⁴⁵ G⁴³ 2460 R⁴⁵ G⁴⁴ 2461 R⁴⁶ G⁴¹ 2462 R⁴⁶ G⁴² 2463 R⁴⁶ G⁴³ 2464 R⁴⁶ G⁴⁴ 2465 R⁴⁷ G⁴¹ 2466 R⁴⁷ G⁴² 2467 R⁴⁷ G⁴³ 2468 R⁴⁷ G⁴⁴ 2469 R⁴⁸ G⁴¹ 2470 R⁴⁸ G⁴² 2471 R⁴⁸ G⁴³ 2472 R⁴⁸ G⁴⁴ 2473 R⁴⁹ G⁴¹ 2474 R⁴⁹ G⁴² 2475 R⁴⁹ G⁴³ 2476 R⁴⁹ G⁴⁴ 2477 R⁵⁰ G⁴¹ 2478 R⁵⁰ G⁴² 2479 R⁵⁰ G⁴³ 2480 R⁵⁰ G⁴⁴ 2481 R⁵¹ G⁴¹ 2482 R⁵¹ G⁴² 2483 R⁵¹ G⁴³ 2484 R⁵¹ G⁴⁴ 2485 R⁵² G⁴¹ 2486 R⁵² G⁴² 2487 R⁵² G⁴³ 2488 R⁵² G⁴⁴ 2489 R⁵³ G⁴¹ 2490 R⁵³ G⁴² 2491 R⁵³ G⁴³ 2492 R⁵³ G⁴⁴ 2493 R⁵⁴ G⁴¹ 2494 R⁵⁴ G⁴² 2495 R⁵⁴ G⁴³ 2496 R⁵⁴ G⁴⁴ 2497 R⁵⁵ G⁴¹ 2498 R⁵⁵ G⁴² 2499 R⁵⁵ G⁴³ 2500 R⁵⁵ G⁴⁴ 2501 R⁵⁶ G⁴¹ 2502 R⁵⁶ G⁴² 2503 R⁵⁶ G⁴³ 2504 R⁵⁶ G⁴⁴ 2505 R⁵⁷ G⁴¹ 2506 R⁵⁷ G⁴² 2507 R⁵⁷ G⁴³ 2508 R⁵⁷ G⁴⁴ 2509 R¹ G⁴⁵ 2510 R¹ G⁴⁶ 2511 R¹ G⁴⁷ 2512 R¹ G⁴⁸ 2513 R² G⁴⁵ 2514 R² G⁴⁶ 2515 R² G⁴⁷ 2516 R² G⁴⁸ 2517 R³ G⁴⁵ 2518 R³ G⁴⁶ 2519 R³ G⁴⁷ 2520 R³ G⁴⁸ 2521 R⁴ G⁴⁵ 2522 R⁴ G⁴⁶ 2523 R⁴ G⁴⁷ 2524 R⁴ G⁴⁸ 2525 R⁵ G⁴⁵ 2526 R⁵ G⁴⁶ 2527 R⁵ G⁴⁷ 2528 R⁵ G⁴⁸ 2529 R⁶ G⁴⁵ 2530 R⁶ G⁴⁶ 2531 R⁶ G⁴⁷ 2532 R⁶ G⁴⁸ 2533 R⁷ G⁴⁵ 2534 R⁷ G⁴⁶ 2535 R⁷ G⁴⁷ 2536 R⁷ G⁴⁸ 2537 R⁸ G⁴⁵ 2538 R⁸ G⁴⁶ 2539 R⁸ G⁴⁷ 2540 R⁸ G⁴⁸ 2541 R⁹ G⁴⁵ 2542 R⁹ G⁴⁶ 2543 R⁹ G⁴⁷ 2544 R⁹ G⁴⁸ 2545 R¹⁰ G⁴⁵ 2546 R¹⁰ G⁴⁶ 2547 R¹⁰ G⁴⁷ 2548 R¹⁰ G⁴⁸ 2549 R¹¹ G⁴⁵ 2550 R¹¹ G⁴⁶ 2551 R¹¹ G⁴⁷ 2552 R¹¹ G⁴⁸ 2553 R¹² G⁴⁵ 2554 R¹² G⁴⁶ 2555 R¹² G⁴⁷ 2556 R¹² G⁴⁸ 2557 R¹³ G⁴⁵ 2558 R¹³ G⁴⁶ 2559 R¹³ G⁴⁷ 2560 R¹³ G⁴⁸ 2561 R¹⁴ G⁴⁵ 2562 R¹⁴ G⁴⁶ 2563 R¹⁴ G⁴⁷ 2564 R¹⁴ G⁴⁸ 2565 R¹⁵ G⁴⁵ 2566 R¹⁵ G⁴⁶ 2567 R¹⁵ G⁴⁷ 2568 R¹⁵ G⁴⁸ 2569 R¹⁶ G⁴⁵ 2570 R¹⁶ G⁴⁶ 2571 R¹⁶ G⁴⁷ 2572 R¹⁶ G⁴⁸ 2573 R¹⁷ G⁴⁵ 2574 R¹⁷ G⁴⁶ 2575 R¹⁷ G⁴⁷ 2576 R¹⁷ G⁴⁸ 2577 R¹⁸ G⁴⁵ 2578 R¹⁸ G⁴⁶ 2579 R¹⁸ G⁴⁷ 2580 R¹⁸ G⁴⁸ 2581 R¹⁹ G⁴⁵ 2582 R¹⁹ G⁴⁶ 2583 R¹⁹ G⁴⁷ 2584 R¹⁹ G⁴⁸ 2585 R²⁰ G⁴⁵ 2586 R²⁰ G⁴⁶ 2587 R²⁰ G⁴⁷ 2588 R²⁰ G⁴⁸ 2589 R²¹ G⁴⁵ 2590 R²¹ G⁴⁶ 2591 R²¹ G⁴⁷ 2592 R²¹ G⁴⁸ 2593 R²² G⁴⁵ 2594 R²² G⁴⁶ 2595 R²² G⁴⁷ 2596 R²² G⁴⁸ 2597 R²³ G⁴⁵ 2598 R²³ G⁴⁶ 2599 R²³ G⁴⁷ 2600 R²³ G⁴⁸ 2601 R²⁴ G⁴⁵ 2602 R²⁴ G⁴⁶ 2603 R²⁴ G⁴⁷ 2604 R²⁴ G⁴⁸ 2605 R²⁵ G⁴⁵ 2606 R²⁵ G⁴⁶ 2607 R²⁵ G⁴⁷ 2608 R²⁵ G⁴⁸ 2609 R²⁶ G⁴⁵ 2610 R²⁶ G⁴⁶ 2611 R²⁶ G⁴⁷ 2612 R²⁶ G⁴⁸ 2613 R²⁷ G⁴⁵ 2614 R²⁷ G⁴⁶ 2615 R²⁷ G⁴⁷ 2616 R²⁷ G⁴⁸ 2617 R²⁸ G⁴⁵ 2618 R²⁸ G⁴⁶ 2619 R²⁸ G⁴⁷ 2620 R²⁸ G⁴⁸ 2621 R²⁹ G⁴⁵ 2622 R²⁹ G⁴⁶ 2623 R²⁹ G⁴⁷ 2624 R²⁹ G⁴⁸ 2625 R³⁰ G⁴⁵ 2626 R³⁰ G⁴⁶ 2627 R³⁰ G⁴⁷ 2628 R³⁰ G⁴⁸ 2629 R³¹ G⁴⁵ 2630 R³¹ G⁴⁶ 2631 R³¹ G⁴⁷ 2632 R³¹ G⁴⁸ 2633 R³² G⁴⁵ 2634 R³² G⁴⁶ 2635 R³² G⁴⁷ 2636 R³² G⁴⁸ 2637 R³³ G⁴⁵ 2638 R³³ G⁴⁶ 2639 R³³ G⁴⁷ 2640 R³³ G⁴⁸ 2641 R³⁴ G⁴⁵ 2642 R³⁴ G⁴⁶ 2643 R³⁴ G⁴⁷ 2644 R³⁴ G⁴⁸ 2645 R³⁵ G⁴⁵ 2646 R³⁵ G⁴⁶ 2647 R³⁵ G⁴⁷ 2648 R³⁵ G⁴⁸ 2649 R³⁶ G⁴⁵ 2650 R³⁶ G⁴⁶ 2651 R³⁶ G⁴⁷ 2652 R³⁶ G⁴⁸ 2653 R³⁷ G⁴⁵ 2654 R³⁷ G⁴⁶ 2655 R³⁷ G⁴⁷ 2656 R³⁷ G⁴⁸ 2657 R³⁸ G⁴⁵ 2658 R³⁸ G⁴⁶ 2659 R³⁸ G⁴⁷ 2660 R³⁸ G⁴⁸ 2661 R³⁹ G⁴⁵ 2662 R³⁹ G⁴⁶ 2663 R³⁹ G⁴⁷ 2664 R³⁹ G⁴⁸ 2665 R⁴⁰ G⁴⁵ 2666 R⁴⁰ G⁴⁶ 2667 R⁴⁰ G⁴⁷ 2668 R⁴⁰ G⁴⁸ 2669 R⁴¹ G⁴⁵ 2670 R⁴¹ G⁴⁶ 2671 R⁴¹ G⁴⁷ 2672 R⁴¹ G⁴⁸ 2673 R⁴² G⁴⁵ 2674 R⁴² G⁴⁶ 2675 R⁴² G⁴⁷ 2676 R⁴² G⁴⁸ 2677 R⁴³ G⁴⁵ 2678 R⁴³ G⁴⁶ 2679 R⁴³ G⁴⁷ 2680 R⁴³ G⁴⁸ 2681 R⁴⁴ G⁴⁵ 2682 R⁴⁴ G⁴⁶ 2683 R⁴⁴ G⁴⁷ 2684 R⁴⁴ G⁴⁸ 2685 R⁴⁵ G⁴⁵ 2686 R⁴⁵ G⁴⁶ 2687 R⁴⁵ G⁴⁷ 2688 R⁴⁵ G⁴⁸ 2689 R⁴⁶ G⁴⁵ 2690 R⁴⁶ G⁴⁶ 2691 R⁴⁶ G⁴⁷ 2692 R⁴⁶ G⁴⁸ 2693 R⁴⁷ G⁴⁵ 2694 R⁴⁷ G⁴⁶ 2695 R⁴⁷ G⁴⁷ 2696 R⁴⁷ G⁴⁸ 2697 R⁴⁸ G⁴⁵ 2698 R⁴⁸ G⁴⁶ 2699 R⁴⁸ G⁴⁷ 2700 R⁴⁸ G⁴⁸ 2701 R⁴⁹ G⁴⁵ 2702 R⁴⁹ G⁴⁶ 2703 R⁴⁹ G⁴⁷ 2704 R⁴⁹ G⁴⁸ 2705 R⁵⁰ G⁴⁵ 2706 R⁵⁰ G⁴⁶ 2707 R⁵⁰ G⁴⁷ 2708 R⁵⁰ G⁴⁸ 2709 R⁵¹ G⁴⁵ 2710 R⁵¹ G⁴⁶ 2711 R⁵¹ G⁴⁷ 2712 R⁵¹ G⁴⁸ 2713 R⁵² G⁴⁵ 2714 R⁵² G⁴⁶ 2715 R⁵² G⁴⁷ 2716 R⁵² G⁴⁸ 2717 R⁵³ G⁴⁵ 2718 R⁵³ G⁴⁶ 2719 R⁵³ G⁴⁷ 2720 R⁵³ G⁴⁸ 2721 R⁵⁴ G⁴⁵ 2722 R⁵⁴ G⁴⁶ 2723 R⁵⁴ G⁴⁷ 2724 R⁵⁴ G⁴⁸ 2725 R⁵⁵ G⁴⁵ 2726 R⁵⁵ G⁴⁶ 2727 R⁵⁵ G⁴⁷ 2728 R⁵⁵ G⁴⁸ 2729 R⁵⁶ G⁴⁵ 2730 R⁵⁶ G⁴⁶ 2731 R⁵⁶ G⁴⁷ 2732 R⁵⁶ G⁴⁸ 2733 R⁵⁷ G⁴⁵ 2734 R⁵⁷ G⁴⁶ 2735 R⁵⁷ G⁴⁷ 2736 R⁵⁷ G⁴⁸ 2737 R¹ G⁴⁹ 2738 R¹ G⁵⁰ 2739 R¹ G⁵¹ 2740 R¹ G⁵² 2741 R² G⁴⁹ 2742 R² G⁵⁰ 2743 R² G⁵¹ 2744 R² G⁵² 2745 R³ G⁴⁹ 2746 R³ G⁵⁰ 2747 R³ G⁵¹ 2748 R³ G⁵² 2749 R⁴ G⁴⁹ 2750 R⁴ G⁵⁰ 2751 R⁴ G⁵¹ 2752 R⁴ G⁵² 2753 R⁵ G⁴⁹ 2754 R⁵ G⁵⁰ 2755 R⁵ G⁵¹ 2756 R⁵ G⁵² 2757 R⁶ G⁴⁹ 2758 R⁶ G⁵⁰ 2759 R⁶ G⁵¹ 2760 R⁶ G⁵² 2761 R⁷ G⁴⁹ 2762 R⁷ G⁵⁰ 2763 R⁷ G⁵¹ 2764 R⁷ G⁵² 2765 R⁸ G⁴⁹ 2766 R⁸ G⁵⁰ 2767 R⁸ G⁵¹ 2768 R⁸ G⁵² 2769 R⁹ G⁴⁹ 2770 R⁹ G⁵⁰ 2771 R⁹ G⁵¹ 2772 R⁹ G⁵² 2773 R¹⁰ G⁴⁹ 2774 R¹⁰ G⁵⁰ 2775 R¹⁰ G⁵¹ 2776 R¹⁰ G⁵² 2777 R¹¹ G⁴⁹ 2778 R¹¹ G⁵⁰ 2779 R¹¹ G⁵¹ 2780 R¹¹ G⁵² 2781 R¹² G⁴⁹ 2782 R¹² G⁵⁰ 2783 R¹² G⁵¹ 2784 R¹² G⁵² 2785 R¹³ G⁴⁹ 2786 R¹³ G⁵⁰ 2787 R¹³ G⁵¹ 2788 R¹³ G⁵² 2789 R¹⁴ G⁴⁹ 2790 R¹⁴ G⁵⁰ 2791 R¹⁴ G⁵¹ 2792 R¹⁴ G⁵² 2793 R¹⁵ G⁴⁹ 2794 R¹⁵ G⁵⁰ 2795 R¹⁵ G⁵¹ 2796 R¹⁵ G⁵² 2797 R¹⁶ G⁴⁹ 2798 R¹⁶ G⁵⁰ 2799 R¹⁶ G⁵¹ 2800 R¹⁶ G⁵² 2801 R¹⁷ G⁴⁹ 2802 R¹⁷ G⁵⁰ 2803 R¹⁷ G⁵¹ 2804 R¹⁷ G⁵² 2805 R¹⁸ G⁴⁹ 2806 R¹⁸ G⁵⁰ 2807 R¹⁸ G⁵¹ 2808 R¹⁸ G⁵² 2809 R¹⁹ G⁴⁹ 2810 R¹⁹ G⁵⁰ 2811 R¹⁹ G⁵¹ 2812 R¹⁹ G⁵² 2813 R²⁰ G⁴⁹ 2814 R²⁰ G⁵⁰ 2815 R²⁰ G⁵¹ 2816 R²⁰ G⁵² 2817 R²¹ G⁴⁹ 2818 R²¹ G⁵⁰ 2819 R²¹ G⁵¹ 2820 R²¹ G⁵² 2821 R²² G⁴⁹ 2822 R²² G⁵⁰ 2823 R²² G⁵¹ 2824 R²² G⁵² 2825 R²³ G⁴⁹ 2826 R²³ G⁵⁰ 2827 R²³ G⁵¹ 2828 R²³ G⁵² 2829 R²⁴ G⁴⁹ 2830 R²⁴ G⁵⁰ 2831 R²⁴ G⁵¹ 2832 R²⁴ G⁵² 2833 R²⁵ G⁴⁹ 2834 R²⁵ G⁵⁰ 2835 R²⁵ G⁵¹ 2836 R²⁵ G⁵² 2837 R²⁶ G⁴⁹ 2838 R²⁶ G⁵⁰ 2839 R²⁶ G⁵¹ 2840 R²⁶ G⁵² 2841 R²⁷ G⁴⁹ 2842 R²⁷ G⁵⁰ 2843 R²⁷ G⁵¹ 2844 R²⁷ G⁵² 2845 R²⁸ G⁴⁹ 2846 R²⁸ G⁵⁰ 2847 R²⁸ G⁵¹ 2848 R²⁸ G⁵² 2849 R²⁹ G⁴⁹ 2850 R²⁹ G⁵⁰ 2851 R²⁹ G⁵¹ 2852 R²⁹ G⁵² 2853 R³⁰ G⁴⁹ 2854 R³⁰ G⁵⁰ 2855 R³⁰ G⁵¹ 2856 R³⁰ G⁵² 2857 R³¹ G⁴⁹ 2858 R³¹ G⁵⁰ 2859 R³¹ G⁵¹ 2860 R³¹ G⁵² 2861 R³² G⁴⁹ 2862 R³² G⁵⁰ 2863 R³² G⁵¹ 2864 R³² G⁵² 2865 R³³ G⁴⁹ 2866 R³³ G⁵⁰ 2867 R³³ G⁵¹ 2868 R³³ G⁵² 2869 R³⁴ G⁴⁹ 2870 R³⁴ G⁵⁰ 2871 R³⁴ G⁵¹ 2872 R³⁴ G⁵² 2873 R³⁵ G⁴⁹ 2874 R³⁵ G⁵⁰ 2875 R³⁵ G⁵¹ 2876 R³⁵ G⁵² 2877 R³⁶ G⁴⁹ 2878 R³⁶ G⁵⁰ 2879 R³⁶ G⁵¹ 2880 R³⁶ G⁵² 2881 R³⁷ G⁴⁹ 2882 R³⁷ G⁵⁰ 2883 R³⁷ G⁵¹ 2884 R³⁷ G⁵² 2885 R³⁸ G⁴⁹ 2886 R³⁸ G⁵⁰ 2887 R³⁸ G⁵¹ 2888 R³⁸ G⁵² 2889 R³⁹ G⁴⁹ 2890 R³⁹ G⁵⁰ 2891 R³⁹ G⁵¹ 2892 R³⁹ G⁵² 2893 R⁴⁰ G⁴⁹ 2894 R⁴⁰ G⁵⁰ 2895 R⁴⁰ G⁵¹ 2896 R⁴⁰ G⁵² 2897 R⁴¹ G⁴⁹ 2898 R⁴¹ G⁵⁰ 2899 R⁴¹ G⁵¹ 2900 R⁴¹ G⁵² 2901 R⁴² G⁴⁹ 2902 R⁴² G⁵⁰ 2903 R⁴² G⁵¹ 2904 R⁴² G⁵² 2905 R⁴³ G⁴⁹ 2906 R⁴³ G⁵⁰ 2907 R⁴³ G⁵¹ 2908 R⁴³ G⁵² 2909 R⁴⁴ G⁴⁹ 2910 R⁴⁴ G⁵⁰ 2911 R⁴⁴ G⁵¹ 2912 R⁴⁴ G⁵² 2913 R⁴⁵ G⁴⁹ 2914 R⁴⁵ G⁵⁰ 2915 R⁴⁵ G⁵¹ 2916 R⁴⁵ G⁵² 2917 R⁴⁶ G⁴⁹ 2918 R⁴⁶ G⁵⁰ 2919 R⁴⁶ G⁵¹ 2920 R⁴⁶ G⁵² 2921 R⁴⁷ G⁴⁹ 2922 R⁴⁷ G⁵⁰ 2923 R⁴⁷ G⁵¹ 2924 R⁴⁷ G⁵² 2925 R⁴⁸ G⁴⁹ 2926 R⁴⁸ G⁵⁰ 2927 R⁴⁸ G⁵¹ 2928 R⁴⁸ G⁵² 2929 R⁴⁹ G⁴⁹ 2930 R⁴⁹ G⁵⁰ 2931 R⁴⁹ G⁵¹ 2932 R⁴⁹ G⁵² 2933 R⁵⁰ G⁴⁹ 2934 R⁵⁰ G⁵⁰ 2935 R⁵⁰ G⁵¹ 2936 R⁵⁰ G⁵² 2937 R⁵¹ G⁴⁹ 2938 R⁵¹ G⁵⁰ 2939 R⁵¹ G⁵¹ 2940 R⁵¹ G⁵² 2941 R⁵² G⁴⁹ 2942 R⁵² G⁵⁰ 2943 R⁵² G⁵¹ 2944 R⁵² G⁵² 2945 R⁵³ G⁴⁹ 2946 R⁵³ G⁵⁰ 2947 R⁵³ G⁵¹ 2948 R⁵³ G⁵² 2949 R⁵⁴ G⁴⁹ 2950 R⁵⁴ G⁵⁰ 2951 R⁵⁴ G⁵¹ 2952 R⁵⁴ G⁵² 2953 R⁵⁵ G⁴⁹ 2954 R⁵⁵ G⁵⁰ 2955 R⁵⁵ G⁵¹ 2956 R⁵⁵ G⁵² 2957 R⁵⁶ G⁴⁹ 2958 R⁵⁶ G⁵⁰ 2959 R⁵⁶ G⁵¹ 2960 R⁵⁶ G⁵² 2961 R⁵⁷ G⁴⁹ 2962 R⁵⁷ G⁵⁰ 2963 R⁵⁷ G⁵¹ 2964 R⁵⁷ G⁵²

where R¹ to R⁵⁷ have the structures in the following LIST 3:

where G¹ to G⁵² have the structures in the following LIST 4:

In some embodiments, the compound has a formula of M(L_(A))_(p)(L_(B))_(q)(L_(C))_(r), wherein L_(B) and L_(C) are each a bidentate ligand; and wherein p is 1, 2, or 3; q is 0, 1, or 2; r is 0, 1, or 2; and p+q+r is the oxidation state of the metal M.

In some embodiments, the compound has a formula selected from the group consisting of Ir(L_(A))₃, Ir(L_(A))(L_(B))₂, Ir(L_(A))₂(L_(B)), Ir(L_(A))₂(L_(C)), and Ir(L_(A))(L_(B))(L_(C)); and wherein L_(A), L_(B), and L_(C) are different from each other.

In some embodiments, L_(B) is a substituted or unsubstituted phenylpyridine, and L_(C) is a substituted or unsubstituted acetylacetonate.

In some embodiments, the compound has a formula of Pt(L_(A))(L_(B)); and wherein L_(A) and L_(B) can be same or different. In some such embodiments, L_(A) and L_(B) are connected to form a tetradentate ligand.

In some embodiments, L_(B) and L_(C) are each independently selected from the group consisting of the structures in the following LIST 5:

wherein:

T is selected from the group consisting of B, Al, Ga, and In;

each of Y¹ to Y¹³ is independently selected from the group consisting of carbon and nitrogen;

Y′ is selected from the group consisting of BR_(e), NR_(e), PR_(e), O, S, Se, C═O, S═O, SO₂, CR_(e)R_(f), SiR_(e)R_(f), and GeR_(e)R_(f);

R_(e) and R_(f) can be fused or joined to form a ring;

each R_(a), R_(b), R_(c), and R_(d) independently represents zero, mono, or up to a maximum allowed number of substitutions to its associated ring;

each of R_(a1), R_(b1), R_(c1), R_(d1), R_(a), R_(b), R_(c), R_(d), R_(e) and R_(f) is independently a hydrogen or a substituent selected from the group consisting of the General Substituents defined herein; and

any two adjacent R_(a), R_(b), R_(c), R_(d), R_(e) and R_(f) can be fused or joined to form a ring or form a multidentate ligand.

In some embodiments, the ligand L_(B) and L_(C) are each independently selected from the group consisting of the structures of the following LIST 6:

wherein:

R_(a)′, R_(b)′, and R_(c)′ each independently represents zero, mono, or up to a maximum allowed number of substitutions to its associated ring;

each of R_(a1), R_(b1), R_(c1), R_(a), R_(b), R_(c), R_(N), R_(a)′, R_(b)′, and R_(c)′ is independently hydrogen or a substituent selected from the group consisting of the Preferred General Substituents defined herein; and

two adjacent R_(a)′, R_(b)′, and R_(c)′ can be fused or joined to form a ring or form a multidentate ligand.

In some embodiments, the compound can have the formula Ir(L_(A))₃, the formula Ir(L_(A))(L_(Bk))₂, the formula Ir(L_(A))₂(L_(Bk)), the formula Ir(L_(A))₂(L_(Cj-I)), the formula Ir(L_(A))₂(L_(Cj-II)), the formula Ir(L_(A))(L_(Bk))(L_(Cj-I)), or the formula Ir(L_(A))(L_(Bk))(L_(Cj-II)), wherein L_(A) is a ligand with respect to Formula I as defined here; L_(Bk) is defined herein; and L_(Cj-I) and L_(Cj-II) are each defined herein.

In some embodiments, when the compound has formula Ir(L_(Ai-m-X))₃, i is an integer from 1 to 2964; m is an integer from 1 to 52; X is an integer from 1 to 4, and the compound is selected from the group consisting of Ir(L_(A1-1-1))₃ to Ir(L_(A2964-52-4))₃;

when the compound has formula Ir(L_(Ai-m-X))(L_(Bk))₂, i is an integer from 1 to 2964; m is an integer from 1 to 52; X is an integer from 1 to 4, k is an integer from 1 to 324; and the compound is selected from the group consisting of Ir(L_(A1-1-1))(L_(B1))₂ to Ir(L_(A2964-52-4))(L_(B324))₂;

when the compound has formula Ir(L_(Ai-m-X))₂(L_(Bk)), i is an integer from 1 to 2964; m is an integer from 1 to 52; X is an integer from 1 to 4, k is an integer from 1 to 324; and the compound is selected from the group consisting of Ir(L_(A1-1-1))₂(L_(B1)) to Ir(L_(A2964-52-4))₂(L_(B324));

when the compound has formula Ir(L_(Ai-m-X))₂(L_(Cj-I)), i is an integer from 1 to 2964; m is an integer from 1 to 52; X is an integer from 1 to 4, j is an integer from 1 to 1416; and the compound is selected from the group consisting of Ir(L_(A1-1-1))₂(L_(Cj-I)) to Ir(L_(A2964-52-4)) (L_(C1416-I)); and

when the compound has formula Ir(L_(Ai-m-X))₂(L_(Cj-II)), i is an integer from 1 to 2964, m is an integer from 1 to 52; X is an integer from 1 to 4, j is an integer from 1 to 1416; and the compound is selected from the group consisting of Ir(L_(A1-1-1))₂(L_(Cj-II)) to Ir(L_(A2964-52-4)) (L_(C1416-II));

wherein each L_(Bk) has the structure defined in the following LIST 7:

wherein each L_(Cj-I) has a structure based on formula

and each L_(Cj-II) has a structure based on formula

wherein for each L_(Cj) in L_(Cj-I) and L_(Cj-II), R²⁰¹ and R²⁰² are each independently defined in the following LIST 8:

L_(Cj) R²⁰¹ R²⁰² L_(Cj) R²⁰¹ R²⁰² L_(Cj) R²⁰¹ R²⁰² L_(Cj) R²⁰¹ R²⁰² L_(C1) R^(D1) R^(D1) L_(C193) R^(D1) R^(D3) L_(C385) R^(D17) R^(D40) L_(C577) R^(D143) R^(D120) L_(C2) R^(D2) R^(D2) L_(C194) R^(D1) R^(D4) L_(C386) R^(D17) R^(D41) L_(C578) R^(D143) R^(D133) L_(C3) R^(D3) R^(D3) L_(C195) R^(D1) R^(D5) L_(C387) R^(D17) R^(D42) L_(C579) R^(D143) R^(D134) L_(C4) R^(D4) R^(D4) L_(C196) R^(D1) R^(D9) L_(C388) R^(D17) R^(D43) L_(C580) R^(D143) R^(D135) L_(C5) R^(D5) R^(D5) L_(C197) R^(D1) R^(D10) L_(C389) R^(D17) R^(D48) L_(C581) R^(D143) R^(D136) L_(C6) R^(D6) R^(D6) L_(C198) R^(D1) R^(D17) L_(C390) R^(D17) R^(D49) L_(C582) R^(D143) R^(D144) L_(C7) R^(D7) R^(D7) L_(C199) R^(D1) R^(D18) L_(C391) R^(D17) R^(D50) L_(C583) R^(D143) R^(D145) L_(C8) R^(D8) R^(D8) L_(C200) R^(D1) R^(D20) L_(C392) R^(D17) R^(D54) L_(C584) R^(D143) R^(D146) L_(C9) R^(D9) R^(D9) L_(C201) R^(D1) R^(D22) L_(C393) R^(D17) R^(D55) L_(C585) R^(D143) R^(D147) L_(C10) R^(D10) R^(D10) L_(C202) R^(D1) R^(D37) L_(C394) R^(D17) R^(D58) L_(C586) R^(D143) R^(D149) L_(C11) R^(D11) R^(D11) L_(C203) R^(D1) R^(D40) L_(C395) R^(D17) R^(D59) L_(C587) R^(D143) R^(D151) L_(C12) R^(D12) R^(D12) L_(C204) R^(D1) R^(D41) L_(C396) R^(D17) R^(D78) L_(C588) R^(D143) R^(D154) L_(C13) R^(D13) R^(D13) L_(C205) R^(D1) R^(D42) L_(C397) R^(D17) R^(D79) L_(C589) R^(D143) R^(D155) L_(C14) R^(D14) R^(D14) L_(C206) R^(D1) R^(D43) L_(C398) R^(D17) R^(D81) L_(C590) R^(D143) R^(D161) L_(C15) R^(D15) R^(D15) L_(C207) R^(D1) R^(D48) L_(C399) R^(D17) R^(D87) L_(C591) R^(D143) R^(D175) L_(C16) R^(D16) R^(D16) L_(C208) R^(D1) R^(D49) L_(C400) R^(D17) R^(D88) L_(C592) R^(D144) R^(D3) L_(C17) R^(D17) R^(D17) L_(C209) R^(D1) R^(D50) L_(C401) R^(D17) R^(D89) L_(C593) R^(D144) R^(D5) L_(C18) R^(D18) R^(D18) L_(C210) R^(D1) R^(D54) L_(C402) R^(D17) R^(D93) L_(C594) R^(D144) R^(D17) L_(C19) R^(D19) R^(D19) L_(C211) R^(D1) R^(D55) L_(C403) R^(D17) R^(D116) L_(C595) R^(D144) R^(D18) L_(C20) R^(D20) R^(D20) L_(C212) R^(D1) R^(D58) L_(C404) R^(D17) R^(D117) L_(C596) R^(D144) R^(D20) L_(C21) R^(D21) R^(D21) L_(C213) R^(D1) R^(D59) L_(C405) R^(D17) R^(D118) L_(C597) R^(D144) R^(D22) L_(C22) R^(D22) R^(D22) L_(C214) R^(D1) R^(D78) L_(C406) R^(D17) R^(D119) L_(C598) R^(D144) R^(D37) L_(C23) R^(D23) R^(D23) L_(C215) R^(D1) R^(D79) L_(C407) R^(D17) R^(D120) L_(C599) R^(D144) R^(D40) L_(C24) R^(D24) R^(D24) L_(C216) R^(D1) R^(D81) L_(C408) R^(D17) R^(D133) L_(C600) R^(D144) R^(D41) L_(C25) R^(D25) R^(D25) L_(C217) R^(D1) R^(D87) L_(C409) R^(D17) R^(D134) L_(C601) R^(D144) R^(D42) L_(C26) R^(D26) R^(D26) L_(C218) R^(D1) R^(D88) L_(C410) R^(D17) R^(D135) L_(C602) R^(D144) R^(D43) L_(C27) R^(D27) R^(D27) L_(C219) R^(D1) R^(D89) L_(C411) R^(D17) R^(D136) L_(C603) R^(D144) R^(D48) L_(C28) R^(D28) R^(D28) L_(C220) R^(D1) R^(D93) L_(C412) R^(D17) R^(D143) L_(C604) R^(D144) R^(D49) L_(C29) R^(D29) R^(D29) L_(C221) R^(D1) R^(D116) L_(C413) R^(D17) R^(D144) L_(C605) R^(D144) R^(D54) L_(C30) R^(D30) R^(D30) L_(C222) R^(D1) R^(D117) L_(C414) R^(D17) R^(D145) L_(C606) R^(D144) R^(D58) L_(C31) R^(D31) R^(D31) L_(C223) R^(D1) R^(D118) L_(C415) R^(D17) R^(D146) L_(C607) R^(D144) R^(D59) L_(C32) R^(D32) R^(D32) L_(C224) R^(D1) R^(D119) L_(C416) R^(D17) R^(D147) L_(C608) R^(D144) R^(D78) L_(C33) R^(D33) R^(D33) L_(C225) R^(D1) R^(D120) L_(C417) R^(D17) R^(D149) L_(C609) R^(D144) R^(D79) L_(C34) R^(D34) R^(D34) L_(C226) R^(D1) R^(D133) L_(C418) R^(D17) R^(D151) L_(C610) R^(D144) R^(D81) L_(C35) R^(D35) R^(D35) L_(C227) R^(D1) R^(D134) L_(C419) R^(D17) R^(D154) L_(C611) R^(D144) R^(D87) L_(C36) R^(D36) R^(D36) L_(C228) R^(D1) R^(D135) L_(C420) R^(D17) R^(D155) L_(C612) R^(D144) R^(D88) L_(C37) R^(D37) R^(D37) L_(C229) R^(D1) R^(D136) L_(C421) R^(D17) R^(D161) L_(C613) R^(D144) R^(D89) L_(C38) R^(D38) R^(D38) L_(C230) R^(D1) R^(D143) L_(C422) R^(D17) R^(D175) L_(C614) R^(D144) R^(D93) L_(C39) R^(D39) R^(D39) L_(C231) R^(D1) R^(D144) L_(C423) R^(D50) R^(D3) L_(C615) R^(D144) R^(D116) L_(C10) R^(D40) R^(D40) L_(C232) R^(D1) R^(D145) L_(C424) R^(D50) R^(D5) L_(C616) R^(D144) R^(D117) L_(C41) R^(D41) R^(D41) L_(C233) R^(D1) R^(D146) L_(C425) R^(D50) R^(D18) L_(C617) R^(D144) R^(D118) L_(C42) R^(D42) R^(D42) L_(C234) R^(D1) R^(D147) L_(C426) R^(D50) R^(D20) L_(C618) R^(D144) R^(D119) L_(C43) R^(D43) R^(D43) L_(C235) R^(D1) R^(D149) L_(C427) R^(D50) R^(D22) L_(C619) R^(D144) R^(D120) L_(C44) R^(D44) R^(D44) L_(C236) R^(D1) R^(D151) L_(C428) R^(D50) R^(D37) L_(C620) R^(D144) R^(D133) L_(C45) R^(D45) R^(D45) L_(C237) R^(D1) R^(D154) L_(C429) R^(D50) R^(D40) L_(C621) R^(D144) R^(D134) L_(C46) R^(D46) R^(D46) L_(C238) R^(D1) R^(D155) L_(C430) R^(D50) R^(D41) L_(C622) R^(D144) R^(D135) L_(C47) R^(D47) R^(D47) L_(C239) R^(D1) R^(D161) L_(C431) R^(D50) R^(D42) L_(C623) R^(D144) R^(D136) L_(C48) R^(D48) R^(D48) L_(C240) R^(D1) R^(D175) L_(C432) R^(D50) R^(D43) L_(C624) R^(D144) R^(D145) L_(C49) R^(D49) R^(D49) L_(C241) R^(D4) R^(D3) L_(C433) R^(D50) R^(D48) L_(C625) R^(D144) R^(D146) L_(C50) R^(D50) R^(D50) L_(C242) R^(D4) R^(D5) L_(C434) R^(D50) R^(D49) L_(C626) R^(D144) R^(D147) L_(C51) R^(D51) R^(D51) L_(C243) R^(D4) R^(D9) L_(C435) R^(D50) R^(D54) L_(C627) R^(D144) R^(D149) L_(C52) R^(D52) R^(D52) L_(C244) R^(D4) R^(D10) L_(C436) R^(D50) R^(D55) L_(C628) R^(D144) R^(D151) L_(C53) R^(D55) R^(D55) L_(C245) R^(D4) R^(D17) L_(C437) R^(D50) R^(D58) L_(C629) R^(D144) R^(D154) L_(C54) R^(D54) R^(D54) L_(C246) R^(D4) R^(D18) L_(C438) R^(D50) R^(D59) L_(C630) R^(D144) R^(D155) L_(C55) R^(D55) R^(D55) L_(C247) R^(D4) R^(D20) L_(C439) R^(D50) R^(D78) L_(C631) R^(D144) R^(D161) L_(C56) R^(D56) R^(D56) L_(C248) R^(D4) R^(D22) L_(C440) R^(D50) R^(D79) L_(C632) R^(D144) R^(D175) L_(C57) R^(D57) R^(D57) L_(C249) R^(D4) R^(D37) L_(C441) R^(D50) R^(D81) L_(C633) R^(D145) R^(D3) L_(C58) R^(D58) R^(D58) L_(C250) R^(D4) R^(D40) L_(C442) R^(D50) R^(D87) L_(C634) R^(D145) R^(D5) L_(C59) R^(D59) R^(D59) L_(C251) R^(D4) R^(D41) L_(C443) R^(D50) R^(D88) L_(C635) R^(D145) R^(D17) L_(C60) R^(D60) R^(D60) L_(C252) R^(D4) R^(D42) L_(C444) R^(D50) R^(D89) L_(C636) R^(D145) R^(D18) L_(C61) R^(D61) R^(D61) L_(C253) R^(D4) R^(D43) L_(C445) R^(D50) R^(D93) L_(C637) R^(D145) R^(D20) L_(C62) R^(D62) R^(D62) L_(C254) R^(D4) R^(D48) L_(C446) R^(D50) R^(D116) L_(C638) R^(D145) R^(D22) L_(C63) R^(D63) R^(D63) L_(C255) R^(D4) R^(D49) L_(C447) R^(D50) R^(D117) L_(C639) R^(D145) R^(D37) L_(C64) R^(D64) R^(D64) L_(C256) R^(D4) R^(D50) L_(C448) R^(D50) R^(D118) L_(C640) R^(D145) R^(D40) L_(C65) R^(D65) R^(D65) L_(C257) R^(D4) R^(D54) L_(C449) R^(D50) R^(D119) L_(C641) R^(D145) R^(D41) L_(C66) R^(D66) R^(D66) L_(C258) R^(D4) R^(D55) L_(C450) R^(D50) R^(D120) L_(C642) R^(D145) R^(D42) L_(C67) R^(D67) R^(D67) L_(C259) R^(D4) R^(D58) L_(C451) R^(D50) R^(D133) L_(C643) R^(D145) R^(D43) L_(C68) R^(D68) R^(D68) L_(C260) R^(D4) R^(D59) L_(C452) R^(D50) R^(D134) L_(C644) R^(D145) R^(D48) L_(C69) R^(D69) R^(D69) L_(C261) R^(D4) R^(D78) L_(C453) R^(D50) R^(D135) L_(C645) R^(D145) R^(D49) L_(C70) R^(D70) R^(D70) L_(C262) R^(D4) R^(D79) L_(C454) R^(D50) R^(D136) L_(C646) R^(D145) R^(D54) L_(C71) R^(D71) R^(D71) L_(C263) R^(D4) R^(D81) L_(C455) R^(D50) R^(D143) L_(C647) R^(D145) R^(D58) L_(C72) R^(D72) R^(D72) L_(C264) R^(D4) R^(D87) L_(C456) R^(D50) R^(D144) L_(C648) R^(D145) R^(D59) L_(C73) R^(D73) R^(D73) L_(C265) R^(D4) R^(D88) L_(C457) R^(D50) R^(D145) L_(C649) R^(D145) R^(D78) L_(C74) R^(D74) R^(D74) L_(C266) R^(D4) R^(D89) L_(C458) R^(D50) R^(D146) L_(C650) R^(D145) R^(D79) L_(C75) R^(D75) R^(D75) L_(C267) R^(D4) R^(D93) L_(C459) R^(D50) R^(D147) L_(C651) R^(D145) R^(D81) L_(C76) R^(D76) R^(D76) L_(C268) R^(D4) R^(D116) L_(C460) R^(D50) R^(D149) L_(C652) R^(D145) R^(D87) L_(C77) R^(D77) R^(D77) L_(C269) R^(D4) R^(D117) L_(C461) R^(D50) R^(D151) L_(C653) R^(D145) R^(D88) L_(C78) R^(D78) R^(D78) L_(C270) R^(D4) R^(D118) L_(C462) R^(D50) R^(D154) L_(C654) R^(D145) R^(D89) L_(C79) R^(D79) R^(D79) L_(C271) R^(D4) R^(D119) L_(C463) R^(D50) R^(D155) L_(C655) R^(D145) R^(D93) L_(C80) R^(D80) R^(D80) L_(C272) R^(D4) R^(D120) L_(C464) R^(D50) R^(D161) L_(C656) R^(D145) R^(D116) L_(C81) R^(D81) R^(D81) L_(C273) R^(D4) R^(D133) L_(C465) R^(D50) R^(D175) L_(C657) R^(D145) R^(D117) L_(C82) R^(D82) R^(D82) L_(C274) R^(D4) R^(D134) L_(C466) R^(D55) R^(D3) L_(C658) R^(D145) R^(D118) L_(C83) R^(D83) R^(D83) L_(C275) R^(D4) R^(D135) L_(C467) R^(D55) R^(D5) L_(C659) R^(D145) R^(D119) L_(C84) R^(D84) R^(D84) L_(C276) R^(D4) R^(D136) L_(C468) R^(D55) R^(D18) L_(C660) R^(D145) R^(D120) L_(C85) R^(D85) R^(D85) L_(C277) R^(D4) R^(D143) L_(C469) R^(D55) R^(D20) L_(C661) R^(D145) R^(D133) L_(C86) R^(D86) R^(D86) L_(C278) R^(D4) R^(D144) L_(C470) R^(D55) R^(D22) L_(C662) R^(D145) R^(D134) L_(C87) R^(D87) R^(D87) L_(C279) R^(D4) R^(D145) L_(C471) R^(D55) R^(D37) L_(C663) R^(D145) R^(D135) L_(C88) R^(D88) R^(D88) L_(C280) R^(D4) R^(D146) L_(C472) R^(D55) R^(D40) L_(C664) R^(D145) R^(D136) L_(C89) R^(D89) R^(D89) L_(C281) R^(D4) R^(D147) L_(C473) R^(D55) R^(D41) L_(C665) R^(D145) R^(D146) L_(C90) R^(D90) R^(D90) L_(C282) R^(D4) R^(D149) L_(C474) R^(D55) R^(D42) L_(C666) R^(D145) R^(D147) L_(C91) R^(D91) R^(D91) L_(C283) R^(D4) R^(D151) L_(C475) R^(D55) R^(D43) L_(C667) R^(D145) R^(D149) L_(C92) R^(D92) R^(D92) L_(C284) R^(D4) R^(D154) L_(C476) R^(D55) R^(D48) L_(C668) R^(D145) R^(D151) L_(C93) R^(D93) R^(D93) L_(C285) R^(D4) R^(D155) L_(C477) R^(D55) R^(D49) L_(C669) R^(D145) R^(D154) L_(C94) R^(D94) R^(D94) L_(C286) R^(D4) R^(D161) L_(C478) R^(D55) R^(D54) L_(C670) R^(D145) R^(D155) L_(C95) R^(D95) R^(D95) L_(C287) R^(D4) R^(D175) L_(C479) R^(D55) R^(D58) L_(C671) R^(D145) R^(D161) L_(C96) R^(D96) R^(D96) L_(C288) R^(D9) R^(D3) L_(C480) R^(D55) R^(D59) L_(C672) R^(D145) R^(D175) L_(C97) R^(D97) R^(D97) L_(C289) R^(D9) R^(D5) L_(C481) R^(D55) R^(D78) L_(C673) R^(D146) R^(D3) L_(C98) R^(D98) R^(D98) L_(C290) R^(D9) R^(D10) L_(C482) R^(D55) R^(D79) L_(C674) R^(D146) R^(D5) L_(C99) R^(D99) R^(D99) L_(C291) R^(D9) R^(D17) L_(C483) R^(D55) R^(D81) L_(C675) R^(D146) R^(D17) L_(C100) R^(D100) R^(D100) L_(C292) R^(D9) R^(D18) L_(C484) R^(D55) R^(D87) L_(C676) R^(D146) R^(D18) L_(C101) R^(D101) R^(D101) L_(C293) R^(D9) R^(D20) L_(C485) R^(D55) R^(D88) L_(C677) R^(D146) R^(D20) L_(C102) R^(D102) R^(D102) L_(C294) R^(D9) R^(D22) L_(C486) R^(D55) R^(D89) L_(C678) R^(D146) R^(D22) L_(C103) R^(D103) R^(D103) L_(C295) R^(D9) R^(D37) L_(C487) R^(D55) R^(D93) L_(C679) R^(D146) R^(D37) L_(C104) R^(D104) R^(D104) L_(C296) R^(D9) R^(D40) L_(C488) R^(D55) R^(D116) L_(C680) R^(D146) R^(D40) L_(C105) R^(D105) R^(D105) L_(C297) R^(D9) R^(D41) L_(C489) R^(D55) R^(D117) L_(C681) R^(D146) R^(D41) L_(C106) R^(D106) R^(D106) L_(C298) R^(D9) R^(D42) L_(C490) R^(D55) R^(D118) L_(C682) R^(D146) R^(D42) L_(C107) R^(D107) R^(D107) L_(C299) R^(D9) R^(D43) L_(C491) R^(D55) R^(D119) L_(C683) R^(D146) R^(D43) L_(C108) R^(D108) R^(D108) L_(C300) R^(D9) R^(D48) L_(C492) R^(D55) R^(D120) L_(C684) R^(D146) R^(D48) L_(C109) R^(D109) R^(D109) L_(C301) R^(D9) R^(D49) L_(C493) R^(D55) R^(D133) L_(C685) R^(D146) R^(D49) L_(C110) R^(D110) R^(D110) L_(C302) R^(D9) R^(D50) L_(C494) R^(D55) R^(D134) L_(C686) R^(D146) R^(D54) L_(C111) R^(D111) R^(D111) L_(C303) R^(D9) R^(D54) L_(C495) R^(D55) R^(D135) L_(C687) R^(D146) R^(D58) L_(C112) R^(D112) R^(D112) L_(C304) R^(D9) R^(D55) L_(C496) R^(D55) R^(D136) L_(C688) R^(D146) R^(D59) L_(C113) R^(D113) R^(D113) L_(C305) R^(D9) R^(D58) L_(C497) R^(D55) R^(D143) L_(C689) R^(D146) R^(D78) L_(C114) R^(D114) R^(D114) L_(C306) R^(D9) R^(D59) L_(C498) R^(D55) R^(D144) L_(C690) R^(D146) R^(D79) L_(C115) R^(D115) R^(D115) L_(C307) R^(D9) R^(D78) L_(C499) R^(D55) R^(D145) L_(C691) R^(D146) R^(D81) L_(C116) R^(D116) R^(D116) L_(C308) R^(D9) R^(D79) L_(C500) R^(D55) R^(D146) L_(C692) R^(D146) R^(D87) L_(C117) R^(D117) R^(D117) L_(C309) R^(D9) R^(D81) L_(C501) R^(D55) R^(D147) L_(C693) R^(D146) R^(D88) L_(C118) R^(D118) R^(D118) L_(C310) R^(D9) R^(D87) L_(C502) R^(D55) R^(D149) L_(C694) R^(D146) R^(D89) L_(C119) R^(D119) R^(D119) L_(C311) R^(D9) R^(D88) L_(C503) R^(D55) R^(D151) L_(C695) R^(D146) R^(D93) L_(C120) R^(D120) R^(D120) L_(C312) R^(D9) R^(D89) L_(C504) R^(D55) R^(D154) L_(C696) R^(D146) R^(D117) L_(C121) R^(D121) R^(D121) L_(C313) R^(D9) R^(D93) L_(C505) R^(D55) R^(D155) L_(C697) R^(D146) R^(D118) L_(C122) R^(D122) R^(D122) L_(C314) R^(D9) R^(D116) L_(C506) R^(D55) R^(D161) L_(C698) R^(D146) R^(D119) L_(C123) R^(D123) R^(D123) L_(C315) R^(D9) R^(D117) L_(C507) R^(D55) R^(D175) L_(C699) R^(D146) R^(D120) L_(C124) R^(D124) R^(D124) L_(C316) R^(D9) R^(D118) L_(C508) R^(D116) R^(D3) L_(C700) R^(D146) R^(D133) L_(C125) R^(D125) R^(D125) L_(C317) R^(D9) R^(D119) L_(C509) R^(D116) R^(D5) L_(C701) R^(D146) R^(D134) L_(C126) R^(D126) R^(D126) L_(C318) R^(D9) R^(D120) L_(C510) R^(D116) R^(D17) L_(C702) R^(D146) R^(D135) L_(C127) R^(D127) R^(D127) L_(C319) R^(D9) R^(D133) L_(C511) R^(D116) R^(D18) L_(C703) R^(D146) R^(D136) L_(C128) R^(D128) R^(D128) L_(C320) R^(D9) R^(D134) L_(C512) R^(D116) R^(D20) L_(C704) R^(D146) R^(D146) L_(C129) R^(D129) R^(D129) L_(C321) R^(D9) R^(D135) L_(C513) R^(D116) R^(D22) L_(C705) R^(D146) R^(D147) L_(C130) R^(D130) R^(D130) L_(C322) R^(D9) R^(D136) L_(C514) R^(D116) R^(D37) L_(C706) R^(D146) R^(D149) L_(C131) R^(D131) R^(D131) L_(C323) R^(D9) R^(D143) L_(C515) R^(D116) R^(D40) L_(C707) R^(D146) R^(D151) L_(C132) R^(D132) R^(D132) L_(C324) R^(D9) R^(D144) L_(C516) R^(D116) R^(D41) L_(C708) R^(D146) R^(D154) L_(C133) R^(D133) R^(D133) L_(C325) R^(D9) R^(D145) L_(C517) R^(D116) R^(D42) L_(C709) R^(D146) R^(D155) L_(C134) R^(D134) R^(D134) L_(C326) R^(D9) R^(D146) L_(C518) R^(D116) R^(D43) L_(C710) R^(D146) R^(D161) L_(C135) R^(D135) R^(D135) L_(C327) R^(D9) R^(D147) L_(C519) R^(D116) R^(D48) L_(C711) R^(D146) R^(D175) L_(C136) R^(D136) R^(D136) L_(C328) R^(D9) R^(D149) L_(C520) R^(D116) R^(D49) L_(C712) R^(D133) R^(D3) L_(C137) R^(D137) R^(D137) L_(C329) R^(D9) R^(D151) L_(C521) R^(D116) R^(D54) L_(C713) R^(D133) R^(D5) L_(C138) R^(D138) R^(D138) L_(C330) R^(D9) R^(D154) L_(C522) R^(D116) R^(D58) L_(C714) R^(D133) R^(D3) L_(C139) R^(D139) R^(D139) L_(C331) R^(D9) R^(D155) L_(C523) R^(D116) R^(D59) L_(C715) R^(D133) R^(D18) L_(C140) R^(D140) R^(D140) L_(C332) R^(D9) R^(D161) L_(C524) R^(D116) R^(D78) L_(C716) R^(D133) R^(D20) L_(C141) R^(D141) R^(D141) L_(C333) R^(D9) R^(D175) L_(C525) R^(D116) R^(D79) L_(C717) R^(D133) R^(D22) L_(C142) R^(D142) R^(D142) L_(C334) R^(D10) R^(D3) L_(C526) R^(D116) R^(D81) L_(C718) R^(D133) R^(D37) L_(C143) R^(D143) R^(D143) L_(C335) R^(D10) R^(D5) L_(C527) R^(D116) R^(D87) L_(C719) R^(D133) R^(D40) L_(C144) R^(D144) R^(D144) L_(C336) R^(D10) R^(D17) L_(C528) R^(D116) R^(D88) L_(C720) R^(D133) R^(D41) L_(C145) R^(D145) R^(D145) L_(C337) R^(D10) R^(D18) L_(C529) R^(D116) R^(D89) L_(C721) R^(D133) R^(D42) L_(C146) R^(D146) R^(D146) L_(C338) R^(D10) R^(D20) L_(C530) R^(D116) R^(D95) L_(C722) R^(D133) R^(D43) L_(C147) R^(D147) R^(D147) L_(C339) R^(D10) R^(D22) L_(C531) R^(D116) R^(D117) L_(C723) R^(D133) R^(D48) L_(C148) R^(D148) R^(D148) L_(C340) R^(D10) R^(D37) L_(C532) R^(D116) R^(D118) L_(C724) R^(D133) R^(D49) L_(C149) R^(D149) R^(D149) L_(C341) R^(D10) R^(D40) L_(C533) R^(D116) R^(D119) L_(C725) R^(D133) R^(D54) L_(C150) R^(D150) R^(D150) L_(C342) R^(D10) R^(D41) L_(C534) R^(D116) R^(D120) L_(C726) R^(D133) R^(D58) L_(C151) R^(D151) R^(D151) L_(C343) R^(D10) R^(D42) L_(C535) R^(D116) R^(D133) L_(C727) R^(D133) R^(D59) L_(C152) R^(D152) R^(D152) L_(C344) R^(D10) R^(D43) L_(C536) R^(D116) R^(D134) L_(C728) R^(D133) R^(D78) L_(C153) R^(D153) R^(D153) L_(C345) R^(D10) R^(D48) L_(C537) R^(D116) R^(D135) L_(C729) R^(D133) R^(D79) L_(C154) R^(D154) R^(D154) L_(C346) R^(D10) R^(D49) L_(C538) R^(D116) R^(D136) L_(C730) R^(D133) R^(D81) L_(C155) R^(D155) R^(D155) L_(C347) R^(D10) R^(D50) L_(C539) R^(D116) R^(D143) L_(C731) R^(D133) R^(D87) L_(C156) R^(D 156) R^(D156) L_(C348) R^(D10) R^(D54) L_(C540) R^(D116) R^(D144) L_(C732) R^(D133) R^(D88) L_(C157) R^(D157) R^(D157) L_(C349) R^(D10) R^(D55) L_(C541) R^(D116) R^(D145) L_(C733) R^(D133) R^(D89) L_(C158) R^(D158) R^(D158) L_(C350) R^(D10) R^(D58) L_(C542) R^(D116) R^(D146) L_(C734) R^(D133) R^(D93) L_(C159) R^(D159) R^(D159) L_(C351) R^(D10) R^(D59) L_(C543) R^(D116) R^(D147) L_(C735) R^(D133) R^(D117) L_(C160) R^(D160) R^(D160) L_(C352) R^(D10) R^(D78) L_(C544) R^(D116) R^(D149) L_(C736) R^(D133) R^(D118) L_(C161) R^(D161) R^(D161) L_(C353) R^(D10) R^(D79) L_(C545) R^(D116) R^(D151) L_(C737) R^(D133) R^(D119) L_(C162) R^(D162) R^(D162) L_(C354) R^(D10) R^(D81) L_(C546) R^(D116) R^(D154) L_(C738) R^(D133) R^(D120) L_(C163) R^(D163) R^(D163) L_(C355) R^(D10) R^(D87) L_(C547) R^(D116) R^(D155) L_(C739) R^(D133) R^(D133) L_(C164) R^(D164) R^(D164) L_(C356) R^(D10) R^(D88) L_(C548) R^(D116) R^(D161) L_(C740) R^(D133) R^(D134) L_(C165) R^(D165) R^(D165) L_(C357) R^(D10) R^(D89) L_(C549) R^(D116) R^(D175) L_(C741) R^(D133) R^(D135) L_(C166) R^(D166) R^(D166) L_(C358) R^(D10) R^(D93) L_(C550) R^(D143) R^(D3) L_(C742) R^(D133) R^(D136) L_(C167) R^(D167) R^(D167) L_(C359) R^(D10) R^(D116) L_(C551) R^(D143) R^(D5) L_(C743) R^(D133) R^(D146) L_(C168) R^(D168) R^(D168) L_(C360) R^(D10) R^(D117) L_(C552) R^(D143) R^(D17) L_(C744) R^(D133) R^(D147) L_(C169) R^(D169) R^(D169) L_(C361) R^(D10) R^(D118) L_(C553) R^(D143) R^(D18) L_(C745) R^(D133) R^(D149) L_(C170) R^(D170) R^(D170) L_(C362) R^(D10) R^(D119) L_(C554) R^(D143) R^(D20) L_(C746) R^(D133) R^(D151) L_(C171) R^(D171) R^(D171) L_(C363) R^(D10) R^(D120) L_(C555) R^(D143) R^(D22) L_(C747) R^(D133) R^(D154) L_(C172) R^(D172) R^(D172) L_(C364) R^(D10) R^(D133) L_(C556) R^(D143) R^(D37) L_(C748) R^(D133) R^(D155) L_(C173) R^(D173) R^(D173) L_(C365) R^(D10) R^(D134) L_(C557) R^(D143) R^(D40) L_(C749) R^(D133) R^(D161) L_(C174) R^(D174) R^(D174) L_(C366) R^(D10) R^(D135) L_(C558) R^(D143) R^(D41) L_(C750) R^(D133) R^(D175) L_(C175) R^(D175) R^(D175) L_(C367) R^(D10) R^(D136) L_(C559) R^(D143) R^(D42) L_(C751) R^(D175) R^(D3) L_(C176) R^(D176) R^(D176) L_(C368) R^(D10) R^(D143) L_(C560) R^(D143) R^(D43) L_(C752) R^(D175) R^(D5) L_(C177) R^(D177) R^(D177) L_(C369) R^(D10) R^(D144) L_(C561) R^(D143) R^(D48) L_(C753) R^(D175) R^(D18) L_(C178) R^(D178) R^(D178) L_(C370) R^(D10) R^(D145) L_(C562) R^(D143) R^(D49) L_(C754) R^(D175) R^(D20) L_(C179) R^(D179) R^(D179) L_(C371) R^(D10) R^(D146) L_(C563) R^(D143) R^(D54) L_(C755) R^(D175) R^(D22) L_(C180) R^(D180) R^(D180) L_(C372) R^(D10) R^(D147) L_(C564) R^(D143) R^(D58) L_(C756) R^(D175) R^(D37) L_(C181) R^(D181) R^(D181) L_(C373) R^(D10) R^(D149) L_(C565) R^(D143) R^(D59) L_(C757) R^(D175) R^(D40) L_(C182) R^(D182) R^(D182) L_(C374) R^(D10) R^(D151) L_(C566) R^(D143) R^(D78) L_(C758) R^(D175) R^(D41) L_(C183) R^(D183) R^(D183) L_(C375) R^(D10) R^(D154) L_(C567) R^(D143) R^(D79) L_(C759) R^(D175) R^(D42) L_(C184) R^(D184) R^(D184) L_(C376) R^(D10) R^(D155) L_(C568) R^(D143) R^(D81) L_(C760) R^(D175) R^(D43) L_(C185) R^(D185) R^(D185) L_(C377) R^(D10) R^(D161) L_(C569) R^(D143) R^(D87) L_(C761) R^(D175) R^(D48) L_(C186) R^(D186) R^(D186) L_(C378) R^(D10) R^(D175) L_(C570) R^(D143) R^(D88) L_(C762) R^(D175) R^(D49) L_(C187) R^(D187) R^(D187) L_(C379) R^(D17) R^(D3) L_(C571) R^(D143) R^(D89) L_(C763) R^(D175) R^(D54) L_(C188) R^(D188) R^(D188) L_(C380) R^(D17) R^(D5) L_(C572) R^(D143) R^(D93) L_(C764) R^(D175) R^(D58) L_(C189) R^(D189) R^(D189) L_(C381) R^(D17) R^(D18) L_(C573) R^(D143) R^(D116) L_(C765) R^(D175) R^(D59) L_(C190) R^(D190) R^(D190) L_(C382) R^(D17) R^(D20) L_(C574) R^(D143) R^(D117) L_(C766) R^(D175) R^(D78) L_(C191) R^(D191) R^(D191) L_(C383) R^(D17) R^(D22) L_(C575) R^(D143) R^(D118) L_(C767) R^(D175) R^(D79) L_(C192) R^(D192) R^(D192) L_(C384) R^(D17) R^(D37) L_(C576) R^(D143) R^(D119) L_(C768) R^(D175) R^(D81) L_(C769) R^(D193) R^(D193) L_(C877) R^(D1) R^(D193) L_(C985) R^(D4) R^(D193) L_(C1093) R^(D9) R^(D193) L_(C770) R^(D194) R^(D194) L_(C878) R^(D1) R^(D194) L_(C986) R^(D4) R^(D194) L_(C1094) R^(D9) R^(D194) L_(C771) R^(D195) R^(D195) L_(C879) R^(D1) R^(D195) L_(C987) R^(D4) R^(D195) L_(C1095) R^(D9) R^(D195) L_(C772) R^(D196) R^(D196) L_(C880) R^(D1) R^(D196) L_(C988) R^(D4) R^(D196) L_(C1096) R^(D9) R^(D196) L_(C773) R^(D197) R^(D197) L_(C881) R^(D1) R^(D197) L_(C989) R^(D4) R^(D197) L_(C1097) R^(D9) R^(D197) L_(C774) R^(D198) R^(D198) L_(C882) R^(D1) R^(D198) L_(C990) R^(D4) R^(D198) L_(C1098) R^(D9) R^(D198) L_(C775) R^(D199) R^(D199) L_(C883) R^(D1) R^(D199) L_(C991) R^(D4) R^(D199) L_(C1099) R^(D9) R^(D199) L_(C776) R^(D200) R^(D200) L_(C884) R^(D1) R^(D200) L_(C992) R^(D4) R^(D200) L_(C1100) R^(D9) R^(D200) L_(C777) R^(D201) R^(D201) L_(C885) R^(D1) R^(D201) L_(C993) R^(D4) R^(D201) L_(C1101) R^(D9) R^(D201) L_(C778) R^(D202) R^(D202) L_(C886) R^(D1) R^(D202) L_(C994) R^(D4) R^(D202) L_(C1102) R^(D9) R^(D202) L_(C779) R^(D203) R^(D203) L_(C887) R^(D1) R^(D203) L_(C995) R^(D4) R^(D203) L_(C1103) R^(D9) R^(D203) L_(C780) R^(D204) R^(D204) L_(C888) R^(D1) R^(D204) L_(C996) R^(D4) R^(D204) L_(C1104) R^(D9) R^(D204) L_(C781) R^(D205) R^(D205) L_(C889) R^(D1) R^(D205) L_(C997) R^(D4) R^(D205) L_(C1105) R^(D9) R^(D205) L_(C782) R^(D206) R^(D206) L_(C890) R^(D1) R^(D206) L_(C998) R^(D4) R^(D206) L_(C1106) R^(D9) R^(D206) L_(C783) R^(D207) R^(D207) L_(C891) R^(D1) R^(D207) L_(C999) R^(D4) R^(D207) L_(C1107) R^(D9) R^(D207) L_(C784) R^(D208) R^(D208) L_(C892) R^(D1) R^(D208) L_(C1000) R^(D4) R^(D208) L_(C1108) R^(D9) R^(D208) L_(C785) R^(D209) R^(D209) L_(C893) R^(D1) R^(D209) L_(C1001) R^(D4) R^(D209) L_(C1109) R^(D9) R^(D209) L_(C786) R^(D210) R^(D210) L_(C894) R^(D1) R^(D210) L_(C1002) R^(D4) R^(D210) L_(C1110) R^(D9) R^(D210) L_(C787) R^(D211) R^(D211) L_(C895) R^(D1) R^(D211) L_(C1003) R^(D4) R^(D211) L_(C1111) R^(D9) R^(D211) L_(C788) R^(D212) R^(D212) L_(C896) R^(D1) R^(D212) L_(C1004) R^(D4) R^(D212) L_(C1112) R^(D9) R^(D212) L_(C789) R^(D213) R^(D213) L_(C897) R^(D1) R^(D213) L_(C1005) R^(D4) R^(D213) L_(C1113) R^(D9) R^(D213) L_(C790) R^(D214) R^(D214) L_(C898) R^(D1) R^(D214) L_(C1006) R^(D4) R^(D214) L_(C1114) R^(D9) R^(D214) L_(C791) R^(D215) R^(D215) L_(C899) R^(D1) R^(D215) L_(C1007) R^(D4) R^(D215) L_(C1115) R^(D9) R^(D215) L_(C792) R^(D216) R^(D216) L_(C900) R^(D1) R^(D216) L_(C1008) R^(D4) R^(D216) L_(C1116) R^(D9) R^(D216) L_(C793) R^(D217) R^(D217) L_(C901) R^(D1) R^(D217) L_(C1009) R^(D4) R^(D217) L_(C1117) R^(D9) R^(D217) L_(C794) R^(D218) R^(D218) L_(C902) R^(D1) R^(D218) L_(C1010) R^(D4) R^(D218) L_(C1118) R^(D9) R^(D218) L_(C795) R^(D219) R^(D219) L_(C903) R^(D1) R^(D219) L_(C1011) R^(D4) R^(D219) L_(C1119) R^(D9) R^(D219) L_(C796) R^(D220) R^(D220) L_(C904) R^(D1) R^(D220) L_(C1012) R^(D4) R^(D220) L_(C1120) R^(D9) R^(D220) L_(C797) R^(D221) R^(D221) L_(C905) R^(D1) R^(D221) L_(C1013) R^(D4) R^(D221) L_(C1121) R^(D9) R^(D221) L_(C798) R^(D222) R^(D222) L_(C906) R^(D1) R^(D222) L_(C1014) R^(D4) R^(D222) L_(C1122) R^(D9) R^(D222) L_(C799) R^(D223) R^(D223) L_(C907) R^(D1) R^(D223) L_(C1015) R^(D4) R^(D223) L_(C1123) R^(D9) R^(D223) L_(C800) R^(D224) R^(D224) L_(C908) R^(D1) R^(D224) L_(C1016) R^(D4) R^(D224) L_(C1124) R^(D9) R^(D224) L_(C801) R^(D225) R^(D225) L_(C909) R^(D1) R^(D225) L_(C1017) R^(D4) R^(D225) L_(C1125) R^(D9) R^(D225) L_(C802) R^(D226) R^(D226) L_(C910) R^(D1) R^(D226) L_(C1018) R^(D4) R^(D226) L_(C1126) R^(D9) R^(D226) L_(C803) R^(D227) R^(D227) L_(C911) R^(D1) R^(D227) L_(C1019) R^(D4) R^(D227) L_(C1127) R^(D9) R^(D227) L_(C804) R^(D228) R^(D228) L_(C912) R^(D1) R^(D228) L_(C1020) R^(D4) R^(D228) L_(C1128) R^(D9) R^(D228) L_(C805) R^(D229) R^(D229) L_(C913) R^(D1) R^(D229) L_(C1021) R^(D4) R^(D229) L_(C1129) R^(D9) R^(D229) L_(C806) R^(D230) R^(D230) L_(C914) R^(D1) R^(D230) L_(C1022) R^(D4) R^(D230) L_(C1130) R^(D9) R^(D230) L_(C807) R^(D231) R^(D231) L_(C915) R^(D1) R^(D231) L_(C1023) R^(D4) R^(D231) L_(C1131) R^(D9) R^(D231) L_(C808) R^(D232) R^(D232) L_(C916) R^(D1) R^(D232) L_(C1024) R^(D4) R^(D232) L_(C1132) R^(D9) R^(D232) L_(C809) R^(D233) R^(D233) L_(C917) R^(D1) R^(D233) L_(C1025) R^(D4) R^(D233) L_(C1133) R^(D9) R^(D233) L_(C810) R^(D234) R^(D234) L_(C918) R^(D1) R^(D234) L_(C1026) R^(D4) R^(D234) L_(C1134) R^(D9) R^(D234) L_(C811) R^(D235) R^(D235) L_(C919) R^(D1) R^(D235) L_(C1027) R^(D4) R^(D235) L_(C1135) R^(D9) R^(D235) L_(C812) R^(D236) R^(D236) L_(C920) R^(D1) R^(D236) L_(C1028) R^(D4) R^(D236) L_(C1136) R^(D9) R^(D236) L_(C813) R^(D237) R^(D237) L_(C921) R^(D1) R^(D237) L_(C1029) R^(D4) R^(D237) L_(C1137) R^(D9) R^(D237) L_(C814) R^(D238) R^(D238) L_(C922) R^(D1) R^(D238) L_(C1030) R^(D4) R^(D238) L_(C1138) R^(D9) R^(D238) L_(C815) R^(D239) R^(D239) L_(C923) R^(D1) R^(D239) L_(C1031) R^(D4) R^(D239) L_(C1139) R^(D9) R^(D239) L_(C816) R^(D240) R^(D240) L_(C924) R^(D1) R^(D240) L_(C1032) R^(D4) R^(D240) L_(C1140) R^(D9) R^(D240) L_(C817) R^(D241) R^(D241) L_(C925) R^(D1) R^(D241) L_(C1033) R^(D4) R^(D241) L_(C1141) R^(D9) R^(D241) L_(C818) R^(D242) R^(D242) L_(C926) R^(D1) R^(D242) L_(C1034) R^(D4) R^(D242) L_(C1142) R^(D9) R^(D242) L_(C819) R^(D243) R^(D243) L_(C927) R^(D1) R^(D243) L_(C1035) R^(D4) R^(D243) L_(C1143) R^(D9) R^(D243) L_(C820) R^(D244) R^(D244) L_(C928) R^(D1) R^(D244) L_(C1036) R^(D4) R^(D244) L_(C1144) R^(D9) R^(D244) L_(C821) R^(D245) R^(D245) L_(C929) R^(D1) R^(D245) L_(C1037) R^(D4) R^(D245) L_(C1145) R^(D9) R^(D245) L_(C822) R^(D246) R^(D246) L_(C930) R^(D1) R^(D246) L_(C1038) R^(D4) R^(D246) L_(C1146) R^(D9) R^(D246) L_(C823) R^(D17) R^(D193) L_(C931) R^(D50) R^(D193) L_(C1039) R^(D145) R^(D193) L_(C1147) R^(D168) R^(D193) L_(C824) R^(D17) R^(D194) L_(C932) R^(D50) R^(D194) L_(C1040) R^(D145) R^(D194) L_(C1148) R^(D168) R^(D194) L_(C825) R^(D17) R^(D195) L_(C933) R^(D50) R^(D195) L_(C1041) R^(D145) R^(D195) L_(C1149) R^(D168) R^(D195) L_(C826) R^(D17) R^(D196) L_(C934) R^(D50) R^(D196) L_(C1042) R^(D145) R^(D196) L_(C1150) R^(D168) R^(D196) L_(C827) R^(D17) R^(D197) L_(C935) R^(D50) R^(D197) L_(C1043) R^(D145) R^(D197) L_(C1151) R^(D168) R^(D197) L_(C828) R^(D17) R^(D198) L_(C936) R^(D50) R^(D198) L_(C1044) R^(D145) R^(D198) L_(C1152) R^(D168) R^(D198) L_(C829) R^(D17) R^(D199) L_(C937) R^(D50) R^(D199) L_(C1045) R^(D145) R^(D199) L_(C1153) R^(D168) R^(D199) L_(C830) R^(D17) R^(D200) L_(C938) R^(D50) R^(D200) L_(C1046) R^(D145) R^(D200) L_(C1154) R^(D168) R^(D200) L_(C831) R^(D17) R^(D201) L_(C939) R^(D50) R^(D201) L_(C1047) R^(D145) R^(D201) L_(C1155) R^(D168) R^(D201) L_(C832) R^(D17) R^(D202) L_(C940) R^(D50) R^(D202) L_(C1048) R^(D145) R^(D202) L_(C1156) R^(D168) R^(D202) L_(C833) R^(D17) R^(D203) L_(C941) R^(D50) R^(D203) L_(C1049) R^(D145) R^(D203) L_(C1157) R^(D168) R^(D203) L_(C834) R^(D17) R^(D204) L_(C942) R^(D50) R^(D204) L_(C1050) R^(D145) R^(D204) L_(C1158) R^(D168) R^(D204) L_(C835) R^(D17) R^(D205) L_(C943) R^(D50) R^(D205) L_(C1051) R^(D145) R^(D205) L_(C1159) R^(D168) R^(D205) L_(C836) R^(D17) R^(D206) L_(C944) R^(D50) R^(D206) L_(C1052) R^(D145) R^(D206) L_(C1160) R^(D168) R^(D206) L_(C837) R^(D17) R^(D207) L_(C945) R^(D50) R^(D207) L_(C1053) R^(D145) R^(D207) L_(C1161) R^(D168) R^(D207) L_(C838) R^(D17) R^(D208) L_(C946) R^(D50) R^(D208) L_(C1054) R^(D145) R^(D208) L_(C1162) R^(D168) R^(D208) L_(C839) R^(D17) R^(D209) L_(C947) R^(D50) R^(D209) L_(C1055) R^(D145) R^(D209) L_(C1163) R^(D168) R^(D209) L_(C840) R^(D17) R^(D210) L_(C948) R^(D50) R^(D210) L_(C1056) R^(D145) R^(D210) L_(C1164) R^(D168) R^(D210) L_(C841) R^(D17) R^(D211) L_(C949) R^(D50) R^(D211) L_(C1057) R^(D145) R^(D211) L_(C1165) R^(D168) R^(D211) L_(C842) R^(D17) R^(D212) L_(C950) R^(D50) R^(D212) L_(C1058) R^(D145) R^(D212) L_(C1166) R^(D168) R^(D212) L_(C843) R^(D17) R^(D213) L_(C951) R^(D50) R^(D213) L_(C1059) R^(D145) R^(D213) L_(C1167) R^(D168) R^(D213) L_(C844) R^(D17) R^(D214) L_(C952) R^(D50) R^(D214) L_(C1060) R^(D145) R^(D214) L_(C1168) R^(D168) R^(D214) L_(C845) R^(D17) R^(D215) L_(C953) R^(D50) R^(D215) L_(C1061) R^(D145) R^(D215) L_(C1169) R^(D168) R^(D215) L_(C846) R^(D17) R^(D216) L_(C954) R^(D50) R^(D216) L_(C1062) R^(D145) R^(D216) L_(C1170) R^(D168) R^(D216) L_(C847) R^(D17) R^(D217) L_(C955) R^(D50) R^(D217) L_(C1063) R^(D145) R^(D217) L_(C1171) R^(D168) R^(D217) L_(C848) R^(D17) R^(D218) L_(C956) R^(D50) R^(D218) L_(C1064) R^(D145) R^(D218) L_(C1172) R^(D168) R^(D218) L_(C849) R^(D17) R^(D219) L_(C957) R^(D50) R^(D219) L_(C1065) R^(D145) R^(D219) L_(C1173) R^(D168) R^(D219) L_(C850) R^(D17) R^(D220) L_(C958) R^(D50) R^(D220) L_(C1066) R^(D145) R^(D220) L_(C1174) R^(D168) R^(D220) L_(C851) R^(D17) R^(D221) L_(C959) R^(D50) R^(D221) L_(C1067) R^(D145) R^(D221) L_(C1175) R^(D168) R^(D221) L_(C852) R^(D17) R^(D222) L_(C960) R^(D50) R^(D222) L_(C1068) R^(D145) R^(D222) L_(C1176) R^(D168) R^(D222) L_(C853) R^(D17) R^(D223) L_(C961) R^(D50) R^(D223) L_(C1069) R^(D145) R^(D223) L_(C1177) R^(D168) R^(D223) L_(C854) R^(D17) R^(D224) L_(C962) R^(D50) R^(D224) L_(C1070) R^(D145) R^(D224) L_(C1178) R^(D168) R^(D224) L_(C855) R^(D17) R^(D225) L_(C963) R^(D50) R^(D225) L_(C1071) R^(D145) R^(D225) L_(C1179) R^(D168) R^(D225) L_(C856) R^(D17) R^(D226) L_(C964) R^(D50) R^(D226) L_(C1072) R^(D145) R^(D226) L_(C1180) R^(D168) R^(D226) L_(C857) R^(D17) R^(D227) L_(C965) R^(D50) R^(D227) L_(C1073) R^(D145) R^(D227) L_(C1181) R^(D168) R^(D227) L_(C858) R^(D17) R^(D228) L_(C966) R^(D50) R^(D228) L_(C1074) R^(D145) R^(D228) L_(C1182) R^(D168) R^(D228) L_(C859) R^(D17) R^(D229) L_(C967) R^(D50) R^(D229) L_(C1075) R^(D145) R^(D229) L_(C1183) R^(D168) R^(D229) L_(C860) R^(D17) R^(D230) L_(C968) R^(D50) R^(D230) L_(C1076) R^(D145) R^(D230) L_(C1184) R^(D168) R^(D230) L_(C861) R^(D17) R^(D231) L_(C969) R^(D50) R^(D231) L_(C1077) R^(D145) R^(D231) L_(C1185) R^(D168) R^(D231) L_(C862) R^(D17) R^(D232) L_(C970) R^(D50) R^(D232) L_(C1078) R^(D145) R^(D232) L_(C1186) R^(D168) R^(D232) L_(C863) R^(D17) R^(D233) L_(C971) R^(D50) R^(D233) L_(C1079) R^(D145) R^(D233) L_(C1187) R^(D168) R^(D233) L_(C864) R^(D17) R^(D234) L_(C972) R^(D50) R^(D234) L_(C1080) R^(D145) R^(D234) L_(C1188) R^(D168) R^(D234) L_(C865) R^(D17) R^(D235) L_(C973) R^(D50) R^(D235) L_(C1081) R^(D145) R^(D235) L_(C1189) R^(D168) R^(D235) L_(C866) R^(D17) R^(D236) L_(C974) R^(D50) R^(D236) L_(C1082) R^(D145) R^(D236) L_(C1190) R^(D168) R^(D236) L_(C867) R^(D17) R^(D237) L_(C975) R^(D50) R^(D237) L_(C1083) R^(D145) R^(D237) L_(C1191) R^(D168) R^(D237) L_(C868) R^(D17) R^(D238) L_(C976) R^(D50) R^(D238) L_(C1084) R^(D145) R^(D238) L_(C1192) R^(D168) R^(D238) L_(C869) R^(D17) R^(D239) L_(C977) R^(D50) R^(D239) L_(C1085) R^(D145) R^(D239) L_(C1193) R^(D168) R^(D239) L_(C870) R^(D17) R^(D240) L_(C978) R^(D50) R^(D240) L_(C1086) R^(D145) R^(D240) L_(C1194) R^(D168) R^(D240) L_(C871) R^(D17) R^(D241) L_(C979) R^(D50) R^(D241) L_(C1087) R^(D145) R^(D241) L_(C1195) R^(D168) R^(D241) L_(C872) R^(D17) R^(D242) L_(C980) R^(D50) R^(D242) L_(C1088) R^(D145) R^(D242) L_(C1196) R^(D168) R^(D242) L_(C873) R^(D17) R^(D243) L_(C981) R^(D50) R^(D243) L_(C1089) R^(D145) R^(D243) L_(C1197) R^(D168) R^(D243) L_(C874) R^(D17) R^(D244) L_(C982) R^(D50) R^(D244) L_(C1090) R^(D145) R^(D244) L_(C1198) R^(D168) R^(D244) L_(C875) R^(D17) R^(D245) L_(C983) R^(D50) R^(D245) L_(C1091) R^(D145) R^(D245) L_(C1199) R^(D168) R^(D245) L_(C876) R^(D17) R^(D246) L_(C984) R^(D50) R^(D246) L_(C1092) R^(D145) R^(D246) L_(C1200) R^(D168) R^(D246) L_(C1201) R^(D10) R^(D193) L_(C1255) R^(D55) R^(D193) L_(C1309) R^(D37) R^(D193) L_(C1363) R^(D143) R^(D193) L_(C1202) R^(D10) R^(D194) L_(C1256) R^(D55) R^(D194) L_(C1310) R^(D37) R^(D194) L_(C1364) R^(D143) R^(D194) L_(C1203) R^(D10) R^(D195) L_(C1257) R^(D55) R^(D195) L_(C1311) R^(D37) R^(D195) L_(C1365) R^(D143) R^(D195) L_(C1204) R^(D10) R^(D196) L_(C1258) R^(D55) R^(D196) L_(C1312) R^(D37) R^(D196) L_(C1366) R^(D143) R^(D196) L_(C1205) R^(D10) R^(D197) L_(C1259) R^(D55) R^(D197) L_(C1313) R^(D37) R^(D197) L_(C1367) R^(D143) R^(D197) L_(C1206) R^(D10) R^(D198) L_(C1260) R^(D55) R^(D198) L_(C1314) R^(D37) R^(D198) L_(C1368) R^(D143) R^(D198) L_(C1207) R^(D10) R^(D199) L_(C1261) R^(D55) R^(D199) L_(C1315) R^(D37) R^(D199) L_(C1369) R^(D143) R^(D199) L_(C1208) R^(D10) R^(D200) L_(C1262) R^(D55) R^(D200) L_(C1316) R^(D37) R^(D200) L_(C1370) R^(D143) R^(D200) L_(C1209) R^(D10) R^(D201) L_(C1263) R^(D55) R^(D201) L_(C1317) R^(D37) R^(D201) L_(C1371) R^(D143) R^(D201) L_(C1210) R^(D10) R^(D202) L_(C1264) R^(D55) R^(D202) L_(C1318) R^(D37) R^(D202) L_(C1372) R^(D143) R^(D202) L_(C1211) R^(D10) R^(D203) L_(C1265) R^(D55) R^(D203) L_(C1319) R^(D37) R^(D203) L_(C1373) R^(D143) R^(D203) L_(C1212) R^(D10) R^(D204) L_(C1266) R^(D55) R^(D204) L_(C1320) R^(D37) R^(D204) L_(C1374) R^(D143) R^(D204) L_(C1213) R^(D10) R^(D205) L_(C1267) R^(D55) R^(D205) L_(C1321) R^(D37) R^(D205) L_(C1375) R^(D143) R^(D205) L_(C1214) R^(D10) R^(D206) L_(C1268) R^(D55) R^(D206) L_(C1322) R^(D37) R^(D206) L_(C1376) R^(D143) R^(D206) L_(C1215) R^(D10) R^(D207) L_(C1269) R^(D55) R^(D207) L_(C1323) R^(D37) R^(D207) L_(C1377) R^(D143) R^(D207) L_(C1216) R^(D10) R^(D208) L_(C1270) R^(D55) R^(D208) L_(C1324) R^(D37) R^(D208) L_(C1378) R^(D143) R^(D208) L_(C1217) R^(D10) R^(D209) L_(C1271) R^(D55) R^(D209) L_(C1325) R^(D37) R^(D209) L_(C1379) R^(D143) R^(D209) L_(C1218) R^(D10) R^(D210) L_(C1272) R^(D55) R^(D210) L_(C1326) R^(D37) R^(D210) L_(C1380) R^(D143) R^(D210) L_(C1219) R^(D10) R^(D211) L_(C1273) R^(D55) R^(D211) L_(C1327) R^(D37) R^(D211) L_(C1381) R^(D143) R^(D211) L_(C1220) R^(D10) R^(D212) L_(C1274) R^(D55) R^(D212) L_(C1328) R^(D37) R^(D212) L_(C1382) R^(D143) R^(D212) L_(C1221) R^(D10) R^(D213) L_(C1275) R^(D55) R^(D213) L_(C1329) R^(D37) R^(D213) L_(C1383) R^(D143) R^(D213) L_(C1222) R^(D10) R^(D214) L_(C1276) R^(D55) R^(D214) L_(C1330) R^(D37) R^(D214) L_(C1384) R^(D143) R^(D214) L_(C1223) R^(D10) R^(D215) L_(C1277) R^(D55) R^(D215) L_(C1331) R^(D37) R^(D215) L_(C1385) R^(D143) R^(D215) L_(C1224) R^(D10) R^(D216) L_(C1278) R^(D55) R^(D216) L_(C1332) R^(D37) R^(D216) L_(C1386) R^(D143) R^(D216) L_(C1225) R^(D10) R^(D217) L_(C1279) R^(D55) R^(D217) L_(C1333) R^(D37) R^(D217) L_(C1387) R^(D143) R^(D217) L_(C1226) R^(D10) R^(D218) L_(C1280) R^(D55) R^(D218) L_(C1334) R^(D37) R^(D218) L_(C1388) R^(D143) R^(D218) L_(C1227) R^(D10) R^(D219) L_(C1281) R^(D55) R^(D219) L_(C1335) R^(D37) R^(D219) L_(C1389) R^(D143) R^(D219) L_(C1228) R^(D10) R^(D220) L_(C1282) R^(D55) R^(D220) L_(C1336) R^(D37) R^(D220) L_(C1390) R^(D143) R^(D220) L_(C1229) R^(D10) R^(D221) L_(C1283) R^(D55) R^(D221) L_(C1337) R^(D37) R^(D221) L_(C1391) R^(D143) R^(D221) L_(C1230) R^(D10) R^(D222) L_(C1284) R^(D55) R^(D222) L_(C1338) R^(D37) R^(D222) L_(C1392) R^(D143) R^(D222) L_(C1231) R^(D10) R^(D223) L_(C1285) R^(D55) R^(D223) L_(C1339) R^(D37) R^(D223) L_(C1393) R^(D143) R^(D223) L_(C1232) R^(D10) R^(D224) L_(C1286) R^(D55) R^(D224) L_(C1340) R^(D37) R^(D224) L_(C1394) R^(D143) R^(D224) L_(C1233) R^(D10) R^(D225) L_(C1287) R^(D55) R^(D225) L_(C1341) R^(D37) R^(D225) L_(C1395) R^(D143) R^(D225) L_(C1234) R^(D10) R^(D226) L_(C1288) R^(D55) R^(D226) L_(C1342) R^(D37) R^(D226) L_(C1396) R^(D143) R^(D226) L_(C1235) R^(D10) R^(D227) L_(C1289) R^(D55) R^(D227) L_(C1343) R^(D37) R^(D227) L_(C1397) R^(D143) R^(D227) L_(C1236) R^(D10) R^(D228) L_(C1290) R^(D55) R^(D228) L_(C1344) R^(D37) R^(D228) L_(C1398) R^(D143) R^(D228) L_(C1237) R^(D10) R^(D229) L_(C1291) R^(D55) R^(D229) L_(C1345) R^(D37) R^(D229) L_(C1399) R^(D143) R^(D229) L_(C1238) R^(D10) R^(D230) L_(C1292) R^(D55) R^(D230) L_(C1346) R^(D37) R^(D230) L_(C1400) R^(D143) R^(D230) L_(C1239) R^(D10) R^(D231) L_(C1293) R^(D55) R^(D231) L_(C1347) R^(D37) R^(D231) L_(C1401) R^(D143) R^(D231) L_(C1240) R^(D10) R^(D232) L_(C1294) R^(D55) R^(D232) L_(C1348) R^(D37) R^(D232) L_(C1402) R^(D143) R^(D232) L_(C1241) R^(D10) R^(D233) L_(C1295) R^(D55) R^(D233) L_(C1349) R^(D37) R^(D233) L_(C1403) R^(D143) R^(D233) L_(C1242) R^(D10) R^(D234) L_(C1296) R^(D55) R^(D234) L_(C1350) R^(D37) R^(D234) L_(C1404) R^(D143) R^(D234) L_(C1243) R^(D10) R^(D235) L_(C1297) R^(D55) R^(D235) L_(C1351) R^(D37) R^(D235) L_(C1405) R^(D143) R^(D235) L_(C1244) R^(D10) R^(D236) L_(C1298) R^(D55) R^(D236) L_(C1352) R^(D37) R^(D236) L_(C1406) R^(D143) R^(D236) L_(C1245) R^(D10) R^(D237) L_(C1299) R^(D55) R^(D237) L_(C1353) R^(D37) R^(D237) L_(C1407) R^(D143) R^(D237) L_(C1246) R^(D10) R^(D238) L_(C1300) R^(D55) R^(D238) L_(C1354) R^(D37) R^(D238) L_(C1408) R^(D143) R^(D238) L_(C1247) R^(D10) R^(D239) L_(C1301) R^(D55) R^(D239) L_(C1355) R^(D37) R^(D239) L_(C1409) R^(D143) R^(D239) L_(C1248) R^(D10) R^(D240) L_(C1302) R^(D55) R^(D240) L_(C1356) R^(D37) R^(D240) L_(C1410) R^(D143) R^(D240) L_(C1249) R^(D10) R^(D241) L_(C1303) R^(D55) R^(D241) L_(C1357) R^(D37) R^(D241) L_(C1411) R^(D143) R^(D241) L_(C1250) R^(D10) R^(D242) L_(C1304) R^(D55) R^(D242) L_(C1358) R^(D37) R^(D242) L_(C1412) R^(D143) R^(D242) L_(C1251) R^(D10) R^(D243) L_(C1305) R^(D55) R^(D243) L_(C1359) R^(D37) R^(D243) L_(C1413) R^(D143) R^(D243) L_(C1252) R^(D10) R^(D244) L_(C1306) R^(D55) R^(D244) L_(C1360) R^(D37) R^(D244) L_(C1414) R^(D143) R^(D244) L_(C1253) R^(D10) R^(D245) L_(C1307) R^(D55) R^(D245) L_(C1361) R^(D37) R^(D245) L_(C1415) R^(D143) R^(D245) L_(C1254) R^(D10) R^(D246) L_(C1308) R^(D55) R^(D246) L_(C1362) R^(D37) R^(D246) L_(C1416) R^(D143) R^(D246)

wherein R^(D1) to R^(D246) have the structures defined in the following LIST 9:

In some embodiments, L_(B) is selected from the group consisting of L_(B1), L_(B2), L_(B18), L_(B28), L_(B38), L_(B108), L_(B118), L_(B122), L_(B124), L_(B126), L_(B128), L_(B130), L_(B132), L_(B134), L_(B136), L_(B138), L_(B140), L_(B142), L_(B144), L_(B156), L_(B158), L_(B160), L_(B162), L_(B164), L_(B168), L_(B172), L_(B175), L_(B204), L_(B206), L_(B214), L_(B216), L_(B218), L_(B220), L_(B222), L_(B231), L_(B233), L_(B235), L_(B237), L_(B240), L_(B242), L_(B244), L_(B246), L_(B248), L_(B250), L_(B252), L_(B254), L_(B256), L_(B258), L_(B260), L_(B262) and L_(B264), L_(B265), L_(B266), L_(B267), L_(B268), L_(B269), and L_(B270).

In some embodiments, L_(B) is selected from the group consisting of L_(B1), L_(B2), L_(B18), L_(B28), L_(B38), L_(B108), L_(B118), L_(B122), L_(B126), L_(B128), L_(B132), L_(B136), L_(B138), L_(B142), L_(B156), L_(B162), L_(B204), L_(B206), L_(B214), L_(B216), L_(B218), L_(B220), L_(B231), L_(B233), L_(B237), L_(B264), L_(B265), L_(B266), L_(B267), L_(B268), L_(B269), and L_(B270).

In some embodiments, L_(Cj-I) and L_(Cj-II) are each independently selected from only those structures in their corresponding group whose corresponding R²⁰¹ and R²⁰² are one of the following structures: R^(D1), R^(D3), R^(D4), R^(D5), R^(D9), R^(D10), R^(D17), R^(D18), R^(D20), R^(D22), R^(D37), R^(D40), R^(D41), R^(D42), R^(D43), R^(D48), R^(D49), R^(D50), R^(D54), R_(D55), R^(D58), R^(D59), R^(D78), R^(D79), R^(D81), R^(D87), R^(D88), R^(D89), R^(D93), R^(D116), R^(D117), R^(D118), R^(D119), R^(D120), R^(D133), R^(D134), R^(D135), R^(D136), R^(D143), R^(D144), R^(D145), R^(D146), R^(D147), R^(D149), R^(D151), R^(D154), R^(D15), R^(D161), R^(D175), R^(D190), R^(D193), R^(D200), R^(D201), R^(D206), R^(D210), R^(D214), R^(D215), R^(D216), R^(D218), R^(D219), R^(D220), R^(D227), R^(D237), R^(D241), R^(D242), R^(D245), and R^(D246).

In some embodiments, L_(Cj-I) and L_(Cj-II) are each independently selected from only those structures in their corresponding group whose corresponding R²⁰¹ and R²⁰² are one of selected from the following structures R^(D1), R^(D3), R^(D4), R^(D5), R^(D9), R^(D10), R^(D17), R^(D22), R^(D43), R^(D50), R^(D78), R^(D116), R^(D118), R^(D133), R^(D134), R^(D135), R^(D136), R^(D143), R^(D144), R^(D145), R^(D146), R^(D149), R^(D151), R^(D154), R^(D155), R^(D190), R^(D193), R^(D200), R^(D201), R^(D206), R^(D210), R^(D214), R^(D215), R^(D216), R^(D218), R^(D219), R^(D220), R^(D227), R^(D237), R^(D241), R^(D242), R^(D245), and R^(D246).

In some embodiments, L_(C) is selected from the group consists of the structures of the following LIST 16:

In some embodiments, the compound is selected from the group consisting of the structures of the following LIST 10:

In some embodiments, the compound has the Formula II:

wherein:

M¹ is Pd or Pt;

moieties E and F are each independently monocyclic or polycyclic ring structure comprising 5-membered and/or 6-membered carbocyclic or heterocyclic rings;

Z¹, Z², X^(3′), and X^(4′) are each independently C or N;

K, K¹, and K² are each independently selected from the group consisting of a direct bond, O, and S, wherein at least two of them are direct bonds;

L¹, L², and L³ are each independently selected from the group consisting of a single bond, absent a bond, O, S, CR′R″, SiR′R″, BR′, and NR′, wherein at least one of L¹ and L² is present;

R^(E) and R^(F) each independently represents zero, mono, or up to a maximum allowed number of substitutions to its associated ring;

each of R′, R″, R^(E), and R^(F) is independently a hydrogen or a substituent selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile, isonitrile, sulfanyl, and combinations thereof; and

two adjacent R^(A), R^(B), R_(C), R^(E), and R^(F) can be joined or fused together to form a ring where chemically feasible.

In some embodiments of Formula II, the up to one of L¹ to L³ is absent a bond. In some embodiments, none of L¹ to L³ is absent a bond.

In some embodiments for Formula II, moiety E and moiety F are both 6-membered aromatic rings.

In some embodiments for Formula II, moiety F is a 5-membered or 6-membered heteroaromatic ring.

In some embodiments for Formula II, L¹ is O or CR′R″.

In some embodiments for Formula II, Z² is N and Z¹ is C. In some embodiments for Formula II, Z² is C and Z¹ is N.

In some embodiments for Formula II, L² is a direct bond. In some embodiments for Formula II, L² is NR′.

In some embodiments for Formula II, K, K¹, and K² are all direct bonds. In some embodiments for Formula II, one of K, K¹, and K² is O.

In some embodiments for Formula II, the compound is selected from the group consisting of compounds having the formula of Pt(L_(A′))(Ly):

wherein L_(A′) is selected from the group consisting of the structures in the following LIST 11:

wherein L_(y) is selected from the group consisting of the structures in the following LIST 12:

wherein R^(G) represents zero, mono, or up to a maximum allowed number of substitutions to its associated ring;

wherein Y′ is selected from the group consisting of O, S, Se, NR^(Y1′), BR^(Y1′), BR^(Y1′)R^(Y1″), CR^(Y1′)R^(Y1″), SiR^(Y1′)R^(Y1″), GeR^(Y1′)R^(Y1″), C═O, C═CR^(Y1′)R^(Y1″) and C═NR^(Y1′), and

each of R^(Y1′), R^(Y1″), R^(G) and R^(X) is independently a hydrogen or a substituent selected from the group consisting of the Preferred General Substituents defined herein.

In some embodiments, the compound is selected from the group consisting of the compounds having the formula of Pt(L_(A′))(Ly):

wherein L_(A′) is selected from the group consisting of L_(A′1)(Ru)(Rv)(Yt), L_(A′2)(Ru)(Rv)(Yt), L_(A′3)(Ru)(Rv)(Yt), L_(A′4)(Ru)(Rv)(Yt), L_(A′5)(Ru)(Rv)(Yt), L_(A′6)(Ru)(Rv)(Yt), L_(A′7)(Ru)(Rv)(Yt), L_(A′8)(Ru)(Rv)(Yt), L_(A′9)(Ru)(Rv)(Yt), L_(A′10)(Ru)(Rv)(Yt), and L_(A′11)(Ru)(Rv)(Yt), below, wherein u is an integer from 1 to 57, v is an integer from 1 to 57, and t is an integer from 1 to 4, and each of L_(A′1)(R1)(R1)(Y1) to L_(A′11)(R57)(R57)(Y4) is defined by the structures in the following LIST 13:

L_(A′) Structure of L_(A′) for L_(A′1)(Ru)(Rv)(Yt), L_(A′1)(R1)(R1)(Y1) to L_(A′1)(R57)(R57)(Y4) have the structure

for L_(A′2)(Ru)(Rv)(Yt), L_(A′2)(R1)(R1)(Y1) to L_(A′2)(R57\(R57)(Y4) have the structure

for L_(A′3)(Ru)(Rv)(Yt), L_(A′3)(R1)(R1)(Y1) to L_(A′3)(R57)(R57)(Y4) have the structure

for L_(A′4)(Ru)(Rv)(Yt), L_(A′4)(R1)(R1)(Y1) to L_(A′4)(R57)(R57)(Y4) have the structure

for L_(A′5)(Ru)(Rv)(Yt), L_(A′5)(R1)(R1)(Y1) to L_(A′5)(R57)(R57)(Y4) have the structure

for L_(A′6)(Ru)(Rv)(Yt), L_(A′6)(R1)(R1)(Y1) to L_(A′6)(R57)(R57)(Y4) have the structure

for L_(A′7)(Ru)(Rv)(Yt), L_(A′7)(R1)(R1)(Y1) to L_(A′7)(R57)(R57(Y4) have the structure

for L_(A′8)(Ru)(Rv)(Yt), L_(A′8)(R1)(R1)(Y1) to L_(A′8)(R57)(R57)(Y4) have the structure

for L_(A′9)(Ru)(Rv)(Yt), L_(A′9)(R1)(R1)(Y1) to L_(A′9)(R57)(R57)(Y4) have the structure

for L_(A′10)(Ru)(Rv)(Yt), L_(A′10)(R1)(R1)(Y1) to L_(A′10)(R57)(R57)(Y4) have the structure

for L_(A′11)(Ru)(Rv)(Yt), L_(A′11)(R1)(R1)(Y1) to L_(A′11)(R57(R57(Y4) have the structure

wherein L_(y) is selected from the group consisting of Ly_(Y1)(Rl)(Rm), L_(Y2)(Rl)(Rm), L_(Y3)(Rn)(Ro)(Yp), L_(Y4)(Rn)(Ro)(Yp), L_(Y5)(Rn)(Ro)(Yp), L_(Y6)(Rn)(Ro)(Yp), L_(Y7)(Rn)(Ro)(Yp), L_(Y8)(Rn)(Ro)(Yp), L_(Y9)(Rn)(Ro)(Yp), L_(Y10)(Rn)(Ro)(Yp), L_(Y11)(Rn)(Ro)(Yp), L_(Y12)(Rn)(Ro)(Yp), L_(Y13)(Rn)(Ro)(Yp), and L_(Y14)(Rn)(Ro),

wherein l is an integer from 1 to 86, m is an integer from 1 to 86, n is an integer from 1 to 57, o is an integer from 1 to 86, and p is an integer from 1 to 4, and each of L_(Y1)(Rl)(Rm) to L_(Y14)(Rn)(Ro) is defined by the structures in the following LIST 14:

L_(Y) Structure of L_(Y) for L_(Y1)(Rl)(Rm), L_(Y1)(R1)(R1) to L_(Y1)(R86)(R86) have the structure

for L_(Y2)(Rl)(Rm), L_(Y2)(R1)(R1) to L_(Y2)(R86)(R86) have the structure

for L_(Y3)(Rn)(Ro)(Yp), L_(Y3)(R1)(R1)(Y1) to L_(Y3)(R57)(R57)(Y4) have the structure

for L_(Y4)(Rn)(Ro)(Yp), L_(Y4)(R1)(R1)(Y1) to L_(Y4)(R57)(R57)(Y4) have the structure

for L_(Y5)(Rn)(Ro)(Yp), L_(Y5)(R1)(R1)(Y1) to L_(Y5)(R57)(R57)(Y4) have the structure

for L_(Y6)(Rn)(Ro)(Yp), L_(Y6)(R1)(R1)(Y1) to L_(Y6)(R57)(R57)(Y4) have the structure

for L_(Y7)(Rn)(Ro)(Yp), L_(Y7)(R1)(R1)(Y1) to L_(Y7)(R57)(R57)(Y4) have the structure

for L_(Y8)(Rn)(Ro)(Yp), L_(Y8)(R1)(R1)(Y1) to L_(Y8)(R57)(R57)(Y4) have the structure

for L_(Y9)(Rn)(Ro)(Yp), L_(Y9)(R1)(R1)Y1) to L_(Y9)(R57)(R57)(Y4) have the structure

for L_(Y10)(Rn)(Rp)(Yp), L_(Y10)(R1)(R1)(Y1) to L_(Y10)(R57)(R57)(Y4) have the structure

for L_(Y11)(Rn)(Ro)(Yp), L_(Y11)(R1)(R1)(Y1) to L_(Y11)(R57)(R57)(Y4) have the structure

for L_(Y12)(Rn)(Ro)(Yp), L_(Y12)(R1)(R1)(Y1) to L_(Y12)(R57)(R57)(Y4) have the structure

for L_(Y13)(Rn)(Ro)(Yp), L_(Y13)(R1)(R1)(Y1) to L_(Y13)(R57)(R57)(Y4) have the structure

for L_(Y14)(Rn)(Ro), L_(Y14)(R1)(R1) to L_(Y14)(R57)(R57) have the structure

wherein Y¹ is O, Y² is S, Y³ is NCH₃, and Y⁴ is Se; and

wherein R¹ to R⁸⁶ have the structures defined in the following LIST 15:

In some embodiments, the compound is selected from the group consisting of the structures of LIST 16:

In some embodiments, the compound having a first ligand L_(A) of Formula I described herein can be at least 30% deuterated, at least 40% deuterated, at least 50% deuterated, at least 60% deuterated, at least 70% deuterated, at least 80% deuterated, at least 90% deuterated, at least 95% deuterated, at least 99% deuterated, or 100% deuterated. As used herein, percent deuteration has its ordinary meaning and includes the percent of possible hydrogen atoms (e.g., positions that are hydrogen, deuterium, or halogen) that are replaced by deuterium atoms.

C. The OLEDs and the Devices of the Present Disclosure

In another aspect, the present disclosure also provides an OLED device comprising an organic layer that contains a compound as disclosed in the above compounds section of the present disclosure.

In some embodiments, the organic layer may comprise a compound comprising a first ligand L_(A) of Formula I as defined herein.

In some embodiments, the organic layer may be an emissive layer and the compound as described herein may be an emissive dopant or a non-emissive dopant.

In some embodiments, the organic layer may further comprise a host, wherein the host comprises a triphenylene containing benzo-fused thiophene or benzo-fused furan, wherein any substituent in the host is an unfused substituent independently selected from the group consisting of C_(n)H_(2n+1), OC_(n)H_(2n+1), OAr₁, N(C_(n)H_(2n+1))₂, N(Ar₁)(Ar₂), CH═CH—C_(n)H_(2n+1), C≡CC_(n)H_(2n+1), Ar₁, Ar₁—Ar₂, C_(n)H_(2n)—Ar₁, or no substitution, wherein n is an integer from 1 to 10; and wherein Ar₁ and Ar₂ are independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof.

In some embodiments, the organic layer may further comprise a host, wherein host comprises at least one chemical moiety selected from the group consisting of triphenylene, carbazole, indolocarbazole, dibenzothiophene, dibenzofuran, dibenzoselenophene, 5λ2-benzo[d]benzo[4,5]imidazo[3,2-a]imidazole, 5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracene, triazine, aza-triphenylene, aza-carbazole, aza-indolocarbazole, aza-dibenzothiophene, aza-dibenzofuran, aza-dibenzoselenophene, aza-5,2-benzo[d]benzo[4,5]imidazo[3,2-a]imidazole, and aza-(5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracene).

In some embodiments, the host may be selected from the HOST Group consisting of:

and combinations thereof.

In some embodiments, the organic layer may further comprise a host, wherein the host comprises a metal complex.

In some embodiments, the compound as described herein may be a sensitizer; wherein the device may further comprise an acceptor; and wherein the acceptor may be selected from the group consisting of fluorescent emitter, delayed fluorescence emitter, and combination thereof.

In yet another aspect, the OLED of the present disclosure may also comprise an emissive region containing a compound as disclosed in the above compounds section of the present disclosure.

In some embodiments, the emissive region may comprise a compound comprising a first ligand L_(A) of Formula I as defined herein.

In some embodiments, at least one of the anode, the cathode, or a new layer disposed over the organic emissive layer functions as an enhancement layer. The enhancement layer comprises a plasmonic material exhibiting surface plasmon resonance that non-radiatively couples to the emitter material and transfers excited state energy from the emitter material to non-radiative mode of surface plasmon polariton. The enhancement layer is provided no more than a threshold distance away from the organic emissive layer, wherein the emitter material has a total non-radiative decay rate constant and a total radiative decay rate constant due to the presence of the enhancement layer and the threshold distance is where the total non-radiative decay rate constant is equal to the total radiative decay rate constant. In some embodiments, the OLED further comprises an outcoupling layer. In some embodiments, the outcoupling layer is disposed over the enhancement layer on the opposite side of the organic emissive layer. In some embodiments, the outcoupling layer is disposed on opposite side of the emissive layer from the enhancement layer but still outcouples energy from the surface plasmon mode of the enhancement layer. The outcoupling layer scatters the energy from the surface plasmon polaritons. In some embodiments this energy is scattered as photons to free space. In other embodiments, the energy is scattered from the surface plasmon mode into other modes of the device such as but not limited to the organic waveguide mode, the substrate mode, or another waveguiding mode. If energy is scattered to the non-free space mode of the OLED other outcoupling schemes could be incorporated to extract that energy to free space. In some embodiments, one or more intervening layer can be disposed between the enhancement layer and the outcoupling layer. The examples for interventing layer(s) can be dielectric materials, including organic, inorganic, perovskites, oxides, and may include stacks and/or mixtures of these materials.

The enhancement layer modifies the effective properties of the medium in which the emitter material resides resulting in any or all of the following: a decreased rate of emission, a modification of emission line-shape, a change in emission intensity with angle, a change in the stability of the emitter material, a change in the efficiency of the OLED, and reduced efficiency roll-off of the OLED device. Placement of the enhancement layer on the cathode side, anode side, or on both sides results in OLED devices which take advantage of any of the above-mentioned effects. In addition to the specific functional layers mentioned herein and illustrated in the various OLED examples shown in the figures, the OLEDs according to the present disclosure may include any of the other functional layers often found in OLEDs.

The enhancement layer can be comprised of plasmonic materials, optically active metamaterials, or hyperbolic metamaterials. As used herein, a plasmonic material is a material in which the real part of the dielectric constant crosses zero in the visible or ultraviolet region of the electromagnetic spectrum. In some embodiments, the plasmonic material includes at least one metal. In such embodiments the metal may include at least one of Ag, Al, Au, Ir, Pt, Ni, Cu, W, Ta, Fe, Cr, Mg, Ga, Rh, Ti, Ru, Pd, In, Bi, Ca alloys or mixtures of these materials, and stacks of these materials. In general, a metamaterial is a medium composed of different materials where the medium as a whole acts differently than the sum of its material parts. In particular, we define optically active metamaterials as materials which have both negative permittivity and negative permeability. Hyperbolic metamaterials, on the other hand, are anisotropic media in which the permittivity or permeability are of different sign for different spatial directions. Optically active metamaterials and hyperbolic metamaterials are strictly distinguished from many other photonic structures such as Distributed Bragg Reflectors (“DBRs”) in that the medium should appear uniform in the direction of propagation on the length scale of the wavelength of light. Using terminology that one skilled in the art can understand: the dielectric constant of the metamaterials in the direction of propagation can be described with the effective medium approximation. Plasmonic materials and metamaterials provide methods for controlling the propagation of light that can enhance OLED performance in a number of ways.

In some embodiments, the enhancement layer is provided as a planar layer. In other embodiments, the enhancement layer has wavelength-sized features that are arranged periodically, quasi-periodically, or randomly, or sub-wavelength-sized features that are arranged periodically, quasi-periodically, or randomly. In some embodiments, the wavelength-sized features and the sub-wavelength-sized features have sharp edges.

In some embodiments, the outcoupling layer has wavelength-sized features that are arranged periodically, quasi-periodically, or randomly, or sub-wavelength-sized features that are arranged periodically, quasi-periodically, or randomly. In some embodiments, the outcoupling layer may be composed of a plurality of nanoparticles and in other embodiments the outcoupling layer is composed of a plurality of nanoparticles disposed over a material. In these embodiments the outcoupling may be tunable by at least one of varying a size of the plurality of nanoparticles, varying a shape of the plurality of nanoparticles, changing a material of the plurality of nanoparticles, adjusting a thickness of the material, changing the refractive index of the material or an additional layer disposed on the plurality of nanoparticles, varying a thickness of the enhancement layer, and/or varying the material of the enhancement layer. The plurality of nanoparticles of the device may be formed from at least one of metal, dielectric material, semiconductor materials, an alloy of metal, a mixture of dielectric materials, a stack or layering of one or more materials, and/or a core of one type of material and that is coated with a shell of a different type of material. In some embodiments, the outcoupling layer is composed of at least metal nanoparticles wherein the metal is selected from the group consisting of Ag, Al, Au, Ir, Pt, Ni, Cu, W, Ta, Fe, Cr, Mg, Ga, Rh, Ti, Ru, Pd, In, Bi, Ca, alloys or mixtures of these materials, and stacks of these materials. The plurality of nanoparticles may have additional layer disposed over them. In some embodiments, the polarization of the emission can be tuned using the outcoupling layer. Varying the dimensionality and periodicity of the outcoupling layer can select a type of polarization that is preferentially outcoupled to air. In some embodiments the outcoupling layer also acts as an electrode of the device.

In yet another aspect, the present disclosure also provides a consumer product comprising an organic light-emitting device (OLED) having an anode; a cathode; and an organic layer disposed between the anode and the cathode, wherein the organic layer may comprise a compound as disclosed in the above compounds section of the present disclosure.

In some embodiments, the consumer product comprises an organic light-emitting device (OLED) having an anode; a cathode; and an organic layer disposed between the anode and the cathode, wherein the organic layer may comprise a compound comprising a first ligand L_(A) of Formula I as defined herein.

In some embodiments, the consumer product can be one of a flat panel display, a computer monitor, a medical monitor, a television, a billboard, a light for interior or exterior illumination and/or signaling, a heads-up display, a fully or partially transparent display, a flexible display, a laser printer, a telephone, a cell phone, tablet, a phablet, a personal digital assistant (PDA), a wearable device, a laptop computer, a digital camera, a camcorder, a viewfinder, a micro-display that is less than 2 inches diagonal, a 3-D display, a virtual reality or augmented reality display, a vehicle, a video wall comprising multiple displays tiled together, a theater or stadium screen, a light therapy device, and a sign.

Generally, an OLED comprises at least one organic layer disposed between and electrically connected to an anode and a cathode. When a current is applied, the anode injects holes and the cathode injects electrons into the organic layer(s). The injected holes and electrons each migrate toward the oppositely charged electrode. When an electron and hole localize on the same molecule, an “exciton,” which is a localized electron-hole pair having an excited energy state, is formed. Light is emitted when the exciton relaxes via a photoemissive mechanism. In some cases, the exciton may be localized on an excimer or an exciplex. Non-radiative mechanisms, such as thermal relaxation, may also occur, but are generally considered undesirable.

Several OLED materials and configurations are described in U.S. Pat. Nos. 5,844,363, 6,303,238, and 5,707,745, which are incorporated herein by reference in their entirety.

The initial OLEDs used emissive molecules that emitted light from their singlet states (“fluorescence”) as disclosed, for example, in U.S. Pat. No. 4,769,292, which is incorporated by reference in its entirety. Fluorescent emission generally occurs in a time frame of less than 10 nanoseconds.

More recently, OLEDs having emissive materials that emit light from triplet states (“phosphorescence”) have been demonstrated. Baldo et al., “Highly Efficient Phosphorescent Emission from Organic Electroluminescent Devices,” Nature, vol. 395, 151-154, 1998; (“Baldo-I”) and Baldo et al., “Very high-efficiency green organic light-emitting devices based on electrophosphorescence,” Appl. Phys. Lett., vol. 75, No. 3, 4-6 (1999) (“Baldo-II”), are incorporated by reference in their entireties. Phosphorescence is described in more detail in U.S. Pat. No. 7,279,704 at cols. 5-6, which are incorporated by reference.

FIG. 1 shows an organic light emitting device 100. The figures are not necessarily drawn to scale. Device 100 may include a substrate 110, an anode 115, a hole injection layer 120, a hole transport layer 125, an electron blocking layer 130, an emissive layer 135, a hole blocking layer 140, an electron transport layer 145, an electron injection layer 150, a protective layer 155, a cathode 160, and a barrier layer 170. Cathode 160 is a compound cathode having a first conductive layer 162 and a second conductive layer 164. Device 100 may be fabricated by depositing the layers described, in order. The properties and functions of these various layers, as well as example materials, are described in more detail in U.S. Pat. No. 7,279,704 at cols. 6-10, which are incorporated by reference.

More examples for each of these layers are available. For example, a flexible and transparent substrate-anode combination is disclosed in U.S. Pat. No. 5,844,363, which is incorporated by reference in its entirety. An example of a p-doped hole transport layer is m-MTDATA doped with F₄-TCNQ at a molar ratio of 50:1, as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference in its entirety. Examples of emissive and host materials are disclosed in U.S. Pat. No. 6,303,238 to Thompson et al., which is incorporated by reference in its entirety. An example of an n-doped electron transport layer is BPhen doped with Li at a molar ratio of 1:1, as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference in its entirety. U.S. Pat. Nos. 5,703,436 and 5,707,745, which are incorporated by reference in their entireties, disclose examples of cathodes including compound cathodes having a thin layer of metal such as Mg:Ag with an overlying transparent, electrically-conductive, sputter-deposited ITO layer. The theory and use of blocking layers is described in more detail in U.S. Pat. No. 6,097,147 and U.S. Patent Application Publication No. 2003/0230980, which are incorporated by reference in their entireties. Examples of injection layers are provided in U.S. Patent Application Publication No. 2004/0174116, which is incorporated by reference in its entirety. A description of protective layers may be found in U.S. Patent Application Publication No. 2004/0174116, which is incorporated by reference in its entirety.

FIG. 2 shows an inverted OLED 200. The device includes a substrate 210, a cathode 215, an emissive layer 220, a hole transport layer 225, and an anode 230. Device 200 may be fabricated by depositing the layers described, in order. Because the most common OLED configuration has a cathode disposed over the anode, and device 200 has cathode 215 disposed under anode 230, device 200 may be referred to as an “inverted” OLED. Materials similar to those described with respect to device 100 may be used in the corresponding layers of device 200. FIG. 2 provides one example of how some layers may be omitted from the structure of device 100.

The simple layered structure illustrated in FIGS. 1 and 2 is provided by way of non-limiting example, and it is understood that embodiments of the present disclosure may be used in connection with a wide variety of other structures. The specific materials and structures described are exemplary in nature, and other materials and structures may be used. Functional OLEDs may be achieved by combining the various layers described in different ways, or layers may be omitted entirely, based on design, performance, and cost factors. Other layers not specifically described may also be included. Materials other than those specifically described may be used. Although many of the examples provided herein describe various layers as comprising a single material, it is understood that combinations of materials, such as a mixture of host and dopant, or more generally a mixture, may be used. Also, the layers may have various sublayers. The names given to the various layers herein are not intended to be strictly limiting. For example, in device 200, hole transport layer 225 transports holes and injects holes into emissive layer 220, and may be described as a hole transport layer or a hole injection layer. In one embodiment, an OLED may be described as having an “organic layer” disposed between a cathode and an anode. This organic layer may comprise a single layer, or may further comprise multiple layers of different organic materials as described, for example, with respect to FIGS. 1 and 2 .

Structures and materials not specifically described may also be used, such as OLEDs comprised of polymeric materials (PLEDs) such as disclosed in U.S. Pat. No. 5,247,190 to Friend et al., which is incorporated by reference in its entirety. By way of further example, OLEDs having a single organic layer may be used. OLEDs may be stacked, for example as described in U.S. Pat. No. 5,707,745 to Forrest et al, which is incorporated by reference in its entirety. The OLED structure may deviate from the simple layered structure illustrated in FIGS. 1 and 2 . For example, the substrate may include an angled reflective surface to improve out-coupling, such as a mesa structure as described in U.S. Pat. No. 6,091,195 to Forrest et al., and/or a pit structure as described in U.S. Pat. No. 5,834,893 to Bulovic et al., which are incorporated by reference in their entireties.

Unless otherwise specified, any of the layers of the various embodiments may be deposited by any suitable method. For the organic layers, preferred methods include thermal evaporation, ink-jet, such as described in U.S. Pat. Nos. 6,013,982 and 6,087,196, which are incorporated by reference in their entireties, organic vapor phase deposition (OVPD), such as described in U.S. Pat. No. 6,337,102 to Forrest et al., which is incorporated by reference in its entirety, and deposition by organic vapor jet printing (OVJP), such as described in U.S. Pat. No. 7,431,968, which is incorporated by reference in its entirety. Other suitable deposition methods include spin coating and other solution based processes. Solution based processes are preferably carried out in nitrogen or an inert atmosphere. For the other layers, preferred methods include thermal evaporation. Preferred patterning methods include deposition through a mask, cold welding such as described in U.S. Pat. Nos. 6,294,398 and 6,468,819, which are incorporated by reference in their entireties, and patterning associated with some of the deposition methods such as ink-jet and organic vapor jet printing (OVJP, also referred to as organic vapor jet deposition (OVJD)). Other methods may also be used. The materials to be deposited may be modified to make them compatible with a particular deposition method. For example, substituents such as alkyl and aryl groups, branched or unbranched, and preferably containing at least 3 carbons, may be used in small molecules to enhance their ability to undergo solution processing. Substituents having 20 carbons or more may be used, and 3-20 carbons are a preferred range. Materials with asymmetric structures may have better solution processability than those having symmetric structures, because asymmetric materials may have a lower tendency to recrystallize. Dendrimer substituents may be used to enhance the ability of small molecules to undergo solution processing.

Devices fabricated in accordance with embodiments of the present disclosure may further optionally comprise a barrier layer. One purpose of the barrier layer is to protect the electrodes and organic layers from damaging exposure to harmful species in the environment including moisture, vapor and/or gases, etc. The barrier layer may be deposited over, under or next to a substrate, an electrode, or over any other parts of a device including an edge. The barrier layer may comprise a single layer, or multiple layers. The barrier layer may be formed by various known chemical vapor deposition techniques and may include compositions having a single phase as well as compositions having multiple phases. Any suitable material or combination of materials may be used for the barrier layer. The barrier layer may incorporate an inorganic or an organic compound or both. The preferred barrier layer comprises a mixture of a polymeric material and a non-polymeric material as described in U.S. Pat. No. 7,968,146, PCT Pat. Application Nos. PCT/US2007/023098 and PCT/US2009/042829, which are herein incorporated by reference in their entireties. To be considered a “mixture”, the aforesaid polymeric and non-polymeric materials comprising the barrier layer should be deposited under the same reaction conditions and/or at the same time. The weight ratio of polymeric to non-polymeric material may be in the range of 95:5 to 5:95. The polymeric material and the non-polymeric material may be created from the same precursor material. In one example, the mixture of a polymeric material and a non-polymeric material consists essentially of polymeric silicon and inorganic silicon.

Devices fabricated in accordance with embodiments of the present disclosure can be incorporated into a wide variety of electronic component modules (or units) that can be incorporated into a variety of electronic products or intermediate components. Examples of such electronic products or intermediate components include display screens, lighting devices such as discrete light source devices or lighting panels, etc. that can be utilized by the end-user product manufacturers. Such electronic component modules can optionally include the driving electronics and/or power source(s). Devices fabricated in accordance with embodiments of the present disclosure can be incorporated into a wide variety of consumer products that have one or more of the electronic component modules (or units) incorporated therein. A consumer product comprising an OLED that includes the compound of the present disclosure in the organic layer in the OLED is disclosed. Such consumer products would include any kind of products that include one or more light source(s) and/or one or more of some type of visual displays. Some examples of such consumer products include flat panel displays, curved displays, computer monitors, medical monitors, televisions, billboards, lights for interior or exterior illumination and/or signaling, heads-up displays, fully or partially transparent displays, flexible displays, rollable displays, foldable displays, stretchable displays, laser printers, telephones, mobile phones, tablets, phablets, personal digital assistants (PDAs), wearable devices, laptop computers, digital cameras, camcorders, viewfinders, micro-displays (displays that are less than 2 inches diagonal), 3-D displays, virtual reality or augmented reality displays, vehicles, video walls comprising multiple displays tiled together, theater or stadium screen, a light therapy device, and a sign. Various control mechanisms may be used to control devices fabricated in accordance with the present disclosure, including passive matrix and active matrix. Many of the devices are intended for use in a temperature range comfortable to humans, such as 18 degrees C. to 30 degrees C., and more preferably at room temperature (20-25° C.), but could be used outside this temperature range, for example, from −40 degree C. to +80° C.

More details on OLEDs, and the definitions described above, can be found in U.S. Pat. No. 7,279,704, which is incorporated herein by reference in its entirety.

The materials and structures described herein may have applications in devices other than OLEDs. For example, other optoelectronic devices such as organic solar cells and organic photodetectors may employ the materials and structures. More generally, organic devices, such as organic transistors, may employ the materials and structures.

In some embodiments, the OLED has one or more characteristics selected from the group consisting of being flexible, being rollable, being foldable, being stretchable, and being curved. In some embodiments, the OLED is transparent or semi-transparent. In some embodiments, the OLED further comprises a layer comprising carbon nanotubes.

In some embodiments, the OLED further comprises a layer comprising a delayed fluorescent emitter. In some embodiments, the OLED comprises a RGB pixel arrangement or white plus color filter pixel arrangement. In some embodiments, the OLED is a mobile device, a hand held device, or a wearable device. In some embodiments, the OLED is a display panel having less than 10 inch diagonal or 50 square inch area. In some embodiments, the OLED is a display panel having at least 10 inch diagonal or 50 square inch area. In some embodiments, the OLED is a lighting panel.

In some embodiments, the compound can be an emissive dopant. In some embodiments, the compound can produce emissions via phosphorescence, fluorescence, thermally activated delayed fluorescence, i.e., TADF (also referred to as E-type delayed fluorescence; see, e.g., U.S. application Ser. No. 15/700,352, which is hereby incorporated by reference in its entirety), triplet-triplet annihilation, or combinations of these processes. In some embodiments, the emissive dopant can be a racemic mixture, or can be enriched in one enantiomer. In some embodiments, the compound can be homoleptic (each ligand is the same). In some embodiments, the compound can be heteroleptic (at least one ligand is different from others). When there are more than one ligand coordinated to a metal, the ligands can all be the same in some embodiments. In some other embodiments, at least one ligand is different from the other ligands. In some embodiments, every ligand can be different from each other. This is also true in embodiments where a ligand being coordinated to a metal can be linked with other ligands being coordinated to that metal to form a tridentate, tetradentate, pentadentate, or hexadentate ligands. Thus, where the coordinating ligands are being linked together, all of the ligands can be the same in some embodiments, and at least one of the ligands being linked can be different from the other ligand(s) in some other embodiments.

In some embodiments, the compound can be used as a phosphorescent sensitizer in an OLED where one or multiple layers in the OLED contains an acceptor in the form of one or more fluorescent and/or delayed fluorescence emitters. In some embodiments, the compound can be used as one component of an exciplex to be used as a sensitizer. As a phosphorescent sensitizer, the compound must be capable of energy transfer to the acceptor and the acceptor will emit the energy or further transfer energy to a final emitter. The acceptor concentrations can range from 0.001% to 100%. The acceptor could be in either the same layer as the phosphorescent sensitizer or in one or more different layers. In some embodiments, the acceptor is a TADF emitter. In some embodiments, the acceptor is a fluorescent emitter. In some embodiments, the emission can arise from any or all of the sensitizer, acceptor, and final emitter.

According to another aspect, a formulation comprising the compound described herein is also disclosed.

The OLED disclosed herein can be incorporated into one or more of a consumer product, an electronic component module, and a lighting panel. The organic layer can be an emissive layer and the compound can be an emissive dopant in some embodiments, while the compound can be a non-emissive dopant in other embodiments.

In yet another aspect of the present disclosure, a formulation that comprises the novel compound disclosed herein is described. The formulation can include one or more components selected from the group consisting of a solvent, a host, a hole injection material, hole transport material, electron blocking material, hole blocking material, and an electron transport material, disclosed herein.

The present disclosure encompasses any chemical structure comprising the novel compound of the present disclosure, or a monovalent or polyvalent variant thereof. In other words, the inventive compound, or a monovalent or polyvalent variant thereof, can be a part of a larger chemical structure. Such chemical structure can be selected from the group consisting of a monomer, a polymer, a macromolecule, and a supramolecule (also known as supermolecule). As used herein, a “monovalent variant of a compound” refers to a moiety that is identical to the compound except that one hydrogen has been removed and replaced with a bond to the rest of the chemical structure. As used herein, a “polyvalent variant of a compound” refers to a moiety that is identical to the compound except that more than one hydrogen has been removed and replaced with a bond or bonds to the rest of the chemical structure. In the instance of a supramolecule, the inventive compound can also be incorporated into the supramolecule complex without covalent bonds.

D. Combination of the Compounds of the Present Disclosure with Other Materials

The materials described herein as useful for a particular layer in an organic light emitting device may be used in combination with a wide variety of other materials present in the device. For example, emissive dopants disclosed herein may be used in conjunction with a wide variety of hosts, transport layers, blocking layers, injection layers, electrodes and other layers that may be present. The materials described or referred to below are non-limiting examples of materials that may be useful in combination with the compounds disclosed herein, and one of skill in the art can readily consult the literature to identify other materials that may be useful in combination.

a) Conductivity Dopants:

A charge transport layer can be doped with conductivity dopants to substantially alter its density of charge carriers, which will in turn alter its conductivity. The conductivity is increased by generating charge carriers in the matrix material, and depending on the type of dopant, a change in the Fermi level of the semiconductor may also be achieved. Hole-transporting layer can be doped by p-type conductivity dopants and n-type conductivity dopants are used in the electron-transporting layer.

Non-limiting examples of the conductivity dopants that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: EP01617493, EP01968131, EP2020694, EP2684932, US20050139810, US20070160905, US20090167167, US2010288362, WO06081780, WO2009003455, WO2009008277, WO2009011327, WO2014009310, US2007252140, US2015060804, US20150123047, and US2012146012.

b) HIL/HTL:

A hole injecting/transporting material to be used in the present disclosure is not particularly limited, and any compound may be used as long as the compound is typically used as a hole injecting/transporting material. Examples of the material include, but are not limited to: a phthalocyanine or porphyrin derivative; an aromatic amine derivative; an indolocarbazole derivative; a polymer containing fluorohydrocarbon; a polymer with conductivity dopants; a conducting polymer, such as PEDOT/PSS; a self-assembly monomer derived from compounds such as phosphonic acid and silane derivatives; a metal oxide derivative, such as MoO_(x); a p-type semiconducting organic compound, such as 1,4,5,8,9,12-Hexaazatriphenylenehexacarbonitrile; a metal complex, and a cross-linkable compounds.

Examples of aromatic amine derivatives used in HIL or HTL include, but not limit to the following general structures:

Each of Ar¹ to Ar⁹ is selected from the group consisting of aromatic hydrocarbon cyclic compounds such as benzene, biphenyl, triphenyl, triphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene; the group consisting of aromatic heterocyclic compounds such as dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine; and the group consisting of 2 to 10 cyclic structural units which are groups of the same type or different types selected from the aromatic hydrocarbon cyclic group and the aromatic heterocyclic group and are bonded to each other directly or via at least one of oxygen atom, nitrogen atom, sulfur atom, silicon atom, phosphorus atom, boron atom, chain structural unit and the aliphatic cyclic group. Each Ar may be unsubstituted or may be substituted by a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acids, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.

In one aspect, Ar¹ to Ar⁹ is independently selected from the group consisting of:

wherein k is an integer from 1 to 20; X¹⁰¹ to X¹⁰⁸ is C (including CH) or N; Z¹⁰¹ is NAr¹, O, or S; Ar¹ has the same group defined above.

Examples of metal complexes used in HIL or HTL include, but are not limited to the following general formula:

wherein Met is a metal, which can have an atomic weight greater than 40; (Y¹⁰¹-Y¹⁰²) is a bidentate ligand, Y¹⁰¹ and Y¹⁰² are independently selected from C, N, O, P, and S; L¹⁰¹ is an ancillary ligand; k′ is an integer value from 1 to the maximum number of ligands that may be attached to the metal; and k′+k″ is the maximum number of ligands that may be attached to the metal.

In one aspect, (Y¹⁰¹-Y¹⁰²) is a 2-phenylpyridine derivative. In another aspect, (Y¹⁰¹-Y¹⁰²) is a carbene ligand. In another aspect, Met is selected from Ir, Pt, Os, and Zn. In a further aspect, the metal complex has a smallest oxidation potential in solution vs. Fc⁺/Fc couple less than about 0.6 V.

Non-limiting examples of the HIL and HTL materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: CN102702075, DE102012005215, EP01624500, EP01698613, EP01806334, EP01930964, EP01972613, EP01997799, EP02011790, EP02055700, EP02055701, EP1725079, EP2085382, EP2660300, EP650955, JP07-073529, JP2005112765, JP2007091719, JP2008021687, JP2014-009196, KR20110088898, KR20130077473, TW201139402, U.S. Ser. No. 06/517,957, US20020158242, US20030162053, US20050123751, US20060182993, US20060240279, US20070145888, US20070181874, US20070278938, US20080014464, US20080091025, US20080106190, US20080124572, US20080145707, US20080220265, US20080233434, US20080303417, US2008107919, US20090115320, US20090167161, US2009066235, US2011007385, US20110163302, US2011240968, US2011278551, US2012205642, US2013241401, US20140117329, US2014183517, U.S. Pat. Nos. 5,061,569, 5,639,914, WO05075451, WO07125714, WO08023550, WO08023759, WO2009145016, WO2010061824, WO2011075644, WO2012177006, WO2013018530, WO2013039073, WO2013087142, WO2013118812, WO2013120577, WO2013157367, WO2013175747, WO2014002873, WO2014015935, WO2014015937, WO2014030872, WO2014030921, WO2014034791, WO2014104514, WO2014157018.

c) EBL:

An electron blocking layer (EBL) may be used to reduce the number of electrons and/or excitons that leave the emissive layer. The presence of such a blocking layer in a device may result in substantially higher efficiencies, and/or longer lifetime, as compared to a similar device lacking a blocking layer. Also, a blocking layer may be used to confine emission to a desired region of an OLED. In some embodiments, the EBL material has a higher LUMO (closer to the vacuum level) and/or higher triplet energy than the emitter closest to the EBL interface. In some embodiments, the EBL material has a higher LUMO (closer to the vacuum level) and/or higher triplet energy than one or more of the hosts closest to the EBL interface. In one aspect, the compound used in EBL contains the same molecule or the same functional groups used as one of the hosts described below.

d) Hosts:

The light emitting layer of the organic EL device of the present disclosure preferably contains at least a metal complex as light emitting material, and may contain a host material using the metal complex as a dopant material. Examples of the host material are not particularly limited, and any metal complexes or organic compounds may be used as long as the triplet energy of the host is larger than that of the dopant. Any host material may be used with any dopant so long as the triplet criteria is satisfied.

Examples of metal complexes used as host are preferred to have the following general formula:

wherein Met is a metal; (Y¹⁰³-Y¹⁰⁴) is a bidentate ligand, Y¹⁰³ and Y¹⁰⁴ are independently selected from C, N, O, P, and S; L¹⁰¹ is an another ligand; k′ is an integer value from 1 to the maximum number of ligands that may be attached to the metal; and k′+k″ is the maximum number of ligands that may be attached to the metal.

In one aspect, the metal complexes are:

wherein (O—N) is a bidentate ligand, having metal coordinated to atoms O and N.

In another aspect, Met is selected from Ir and Pt. In a further aspect, (Y¹⁰³-Y¹⁰⁴) is a carbene ligand.

In one aspect, the host compound contains at least one of the following groups selected from the group consisting of aromatic hydrocarbon cyclic compounds such as benzene, biphenyl, triphenyl, triphenylene, tetraphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene; the group consisting of aromatic heterocyclic compounds such as dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine; and the group consisting of 2 to 10 cyclic structural units which are groups of the same type or different types selected from the aromatic hydrocarbon cyclic group and the aromatic heterocyclic group and are bonded to each other directly or via at least one of oxygen atom, nitrogen atom, sulfur atom, silicon atom, phosphorus atom, boron atom, chain structural unit and the aliphatic cyclic group. Each option within each group may be unsubstituted or may be substituted by a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acids, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.

In one aspect, the host compound contains at least one of the following groups in the molecule:

wherein R¹⁰¹ is selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acids, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, and when it is aryl or heteroaryl, it has the similar definition as Ar's mentioned above. k is an integer from 0 to 20 or 1 to 20. X¹⁰¹ to X¹⁰⁸ are independently selected from C (including CH) or N. Z¹⁰¹ and Z¹⁰² are independently selected from NR¹⁰¹, O, or S.

Non-limiting examples of the host materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: EP2034538, EP2034538A, EP2757608, JP2007254297, KR20100079458, KR20120088644, KR20120129733, KR20130115564, TW201329200, US20030175553, US20050238919, US20060280965, US20090017330, US20090030202, US20090167162, US20090302743, US20090309488, US20100012931, US20100084966, US20100187984, US2010187984, US2012075273, US2012126221, US2013009543, US2013105787, US2013175519, US2014001446, US20140183503, US20140225088, US2014034914, U.S. Pat. No. 7,154,114, WO2001039234, WO2004093207, WO2005014551, WO2005089025, WO2006072002, WO2006114966, WO2007063754, WO2008056746, WO2009003898, WO2009021126, WO2009063833, WO2009066778, WO2009066779, WO2009086028, WO2010056066, WO2010107244, WO2011081423, WO2011081431, WO2011086863, WO2012128298, WO2012133644, WO2012133649, WO2013024872, WO2013035275, WO2013081315, WO2013191404, WO2014142472, US20170263869, US20160163995, U.S. Pat. No. 9,466,803,

e) Additional Emitters:

One or more additional emitter dopants may be used in conjunction with the compound of the present disclosure. Examples of the additional emitter dopants are not particularly limited, and any compounds may be used as long as the compounds are typically used as emitter materials. Examples of suitable emitter materials include, but are not limited to, compounds which can produce emissions via phosphorescence, fluorescence, thermally activated delayed fluorescence, i.e., TADF (also referred to as E-type delayed fluorescence), triplet-triplet annihilation, or combinations of these processes.

Non-limiting examples of the emitter materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: CN103694277, CN1696137, EB01238981, EP01239526, EP01961743, EP1239526, EP1244155, EP1642951, EP1647554, EP1841834, EP1841834B, EP2062907, EP2730583, JP2012074444, JP2013110263, JP4478555, KR1020090133652, KR20120032054, KR20130043460, TW201332980, U.S. Ser. No. 06/699,599, U.S. Ser. No. 06/916,554, US20010019782, US20020034656, US20030068526, US20030072964, US20030138657, US20050123788, US20050244673, US2005123791, US2005260449, US20060008670, US20060065890, US20060127696, US20060134459, US20060134462, US20060202194, US20060251923, US20070034863, US20070087321, US20070103060, US20070111026, US20070190359, US20070231600, US2007034863, US2007104979, US2007104980, US2007138437, US2007224450, US2007278936, US20080020237, US20080233410, US20080261076, US20080297033, US200805851, US2008161567, US2008210930, US20090039776, US20090108737, US20090115322, US20090179555, US2009085476, US2009104472, US20100090591, US20100148663, US20100244004, US20100295032, US2010102716, US2010105902, US2010244004, US2010270916, US20110057559, US20110108822, US20110204333, US2011215710, US2011227049, US2011285275, US2012292601, US20130146848, US2013033172, US2013165653, US2013181190, US2013334521, US20140246656, US2014103305, U.S. Pat. Nos. 6,303,238, 6,413,656, 6,653,654, 6,670,645, 6,687,266, 6,835,469, 6,921,915, 7,279,704, 7,332,232, 7,378,162, 7,534,505, 7,675,228, 7,728,137, 7,740,957, 7,759,489, 7,951,947, 8,067,099, 8,592,586, 8,871,361, WO06081973, WO06121811, WO07018067, WO07108362, WO07115970, WO07115981, WO08035571, WO2002015645, WO2003040257, WO2005019373, WO2006056418, WO2008054584, WO2008078800, WO2008096609, WO2008101842, WO2009000673, WO2009050281, WO2009100991, WO2010028151, WO2010054731, WO2010086089, WO2010118029, WO2011044988, WO2011051404, WO2011107491, WO2012020327, WO2012163471, WO2013094620, WO2013107487, WO2013174471, WO2014007565, WO2014008982, WO2014023377, WO2014024131, WO2014031977, WO2014038456, WO2014112450.

f) HBL:

A hole blocking layer (HBL) may be used to reduce the number of holes and/or excitons that leave the emissive layer. The presence of such a blocking layer in a device may result in substantially higher efficiencies and/or longer lifetime as compared to a similar device lacking a blocking layer. Also, a blocking layer may be used to confine emission to a desired region of an OLED. In some embodiments, the HBL material has a lower HOMO (further from the vacuum level) and/or higher triplet energy than the emitter closest to the HBL interface. In some embodiments, the HBL material has a lower HOMO (further from the vacuum level) and/or higher triplet energy than one or more of the hosts closest to the HBL interface.

In one aspect, compound used in HBL contains the same molecule or the same functional groups used as host described above.

In another aspect, compound used in HBL contains at least one of the following groups in the molecule:

wherein k is an integer from 1 to 20; L¹⁰¹ is another ligand, k′ is an integer from 1 to 3.

g) ETL:

Electron transport layer (ETL) may include a material capable of transporting electrons. Electron transport layer may be intrinsic (undoped), or doped. Doping may be used to enhance conductivity. Examples of the ETL material are not particularly limited, and any metal complexes or organic compounds may be used as long as they are typically used to transport electrons.

In one aspect, compound used in ETL contains at least one of the following groups in the molecule:

wherein R¹⁰¹ is selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acids, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, when it is aryl or heteroaryl, it has the similar definition as Ar's mentioned above. Ar¹ to Ar³ has the similar definition as Ar's mentioned above. k is an integer from 1 to 20. X¹⁰¹ to X¹⁰⁸ is selected from C (including CH) or N.

In another aspect, the metal complexes used in ETL contains, but not limit to the following general formula:

wherein (O—N) or (N—N) is a bidentate ligand, having metal coordinated to atoms O, N or N, N; L¹⁰¹ is another ligand; k′ is an integer value from 1 to the maximum number of ligands that may be attached to the metal.

Non-limiting examples of the ETL materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: CN103508940, EP01602648, EP01734038, EP01956007, JP2004-022334, JP2005149918, JP2005-268199, KR0117693, KR20130108183, US20040036077, US20070104977, US2007018155, US20090101870, US20090115316, US20090140637, US20090179554, US2009218940, US2010108990, US2011156017, US2011210320, US2012193612, US2012214993, US2014014925, US2014014927, US20140284580, U.S. Pat. Nos. 6,656,612, 8,415,031, WO2003060956, WO2007111263, WO2009148269, WO2010067894, WO2010072300, WO2011074770, WO2011105373, WO2013079217, WO2013145667, WO2013180376, WO2014104499, WO2014104535,

h) Charge Generation Layer (CGL)

In tandem or stacked OLEDs, the CGL plays an essential role in the performance, which is composed of an n-doped layer and a p-doped layer for injection of electrons and holes, respectively. Electrons and holes are supplied from the CGL and electrodes. The consumed electrons and holes in the CGL are refilled by the electrons and holes injected from the cathode and anode, respectively; then, the bipolar currents reach a steady state gradually. Typical CGL materials include n and p conductivity dopants used in the transport layers.

In any above-mentioned compounds used in each layer of the OLED device, the hydrogen atoms can be partially or fully deuterated. The minimum amount of hydrogen of the compound being deuterated is selected from the group consisting of 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, and 100%. Thus, any specifically listed substituent, such as, without limitation, methyl, phenyl, pyridyl, etc. may be undeuterated, partially deuterated, and fully deuterated versions thereof. Similarly, classes of substituents such as, without limitation, alkyl, aryl, cycloalkyl, heteroaryl, etc. also may be undeuterated, partially deuterated, and fully deuterated versions thereof.

It is understood that the various embodiments described herein are by way of example only and are not intended to limit the scope of the invention. For example, many of the materials and structures described herein may be substituted with other materials and structures without deviating from the spirit of the invention. The present invention as claimed may therefore include variations from the particular examples and preferred embodiments described herein, as will be apparent to one of skill in the art. It is understood that various theories as to why the invention works are not intended to be limiting.

Experimental Data

1-Bromo-3-chloro-2-(trifluoromethyl)benzene (20 g, 77 mmol) and DIPEA (33.7 ml, 193 mmol) were dissolved in dry dioxane (300 mL) under nitrogen and degassed with nitrogen for 30 minutes. 2-ethylhexyl 3-mercaptopropanoate (21.1 mL, 93 mmol) and XantPhos Pd G3 (3.3 g, 3.48 mmol) were added and the reaction mixture was heated to 80° C. for 18 hours. The reaction mixture was cooled to room temperature (RT), diluted with DCM (240 mL), the solids were filtered off and the filtrate concentrated in vacuo to give an orange oily solid. This was purified on the CombiFlash (2×330 g silica columns, eluted with 0-10% EtOAc in isohexane, dry loaded on silica) to afford a pale yellow oil, 2-ethylhexyl 3-((3-chloro-2-(trifluoromethyl)phenyl)thio)propanoate (18.6 g, 58% yield).

2-Ethylhexyl 3-((3-chloro-2-(trifluoromethyl)phenyl)thio)propanoate (18.6 g, 44.5 mmol) was dissolved in toluene (180 mL) and EtOH (180 mL) under nitrogen. Then, sodium ethoxide (21 wt % in EtOH) (49.9 mL, 134 mmol) was added and the reaction mixture stirred at RT for 18 hours. The reaction mixture was quenched with 0.5 M HCl (300 mL), extracted with EtOAc (600 mL), the organics washed with water (150 ml), dried over MgSO₄, filtered and concentrated in vacuo (down to 75 mbar at 40° C.) to give an orange-brown oil. This was purified on the CombiFlash (330 g silica column, eluted with 0-10% EtOAc in isohexane, dry loaded on silica) to afford a colourless oil, 3-chloro-2-(trifluoromethyl)benzenethiol (7.61 g, 73% yield). This was stored under nitrogen until use in the next step.

2-Chloro-3-iodopyridin-4-amine (6.0 g, 23.58 mmol), 3-chloro-2-(trifluoromethyl)benzenethiol (7.31 g, 32.7 mmol), ethylene glycol (3.02 mL, 54.2 mmol) and potassium carbonate (anhydrous powder) (6.52 g, 47.2 mmol) were suspended in dry 2-propanol (120 mL) under nitrogen and degassed for 20 minutes. Copper(I) iodide (0.449 g, 2.358 mmol) was added and the reaction mixture heated at 80° C. for 18 hours. The reaction mixture was cooled to RT and concentrated under reduced pressure to give a cream solid. This was purified on the CombiFlash (330 g silica column, eluted with 10-80% EtOAc in isohexane, dry loaded on silica) to afford a white solid, 2-chloro-3-((3-chloro-2-(trifluoromethyl)phenyl)thio)pyridin-4-amine (4.61 g, 55% yield).

2-Chloro-3-((3-chloro-2-(trifluoromethyl)phenyl)thio)pyridin-4-amine (8.88 g, 24.87 mmol) was dissolved in acetic acid (180 mL) in an open flask, tert-butyl nitrite (4.31 mL, 32.3 mmol) was added slowly over 5 min and the mixture stirred at RT for 4 hours. The reaction mixture was poured into ice-water mixture (350 mL) and then stirred for 1 hour. The resulting precipitate was collected by filtration and washed with water (3×75 mL), sat. NaHCO₃ (75 mL) and isohexane (75 mL). The solid was dried in vacuo to give an orange solid. This was suspended in MtBE (75 mL), sonicated for 5 min, then stirred at RT for 60 hours. The solids were filtered off, washed with isohexane (25 mL), dried in vacuo to give a pale orange solid, 1,7-dichloro-8-(trifluoromethyl)benzo[4,5]thieno[2,3-c]pyridine (5.26 g, 63%).

1,7-Dichloro-8-(trifluoromethyl)benzo[4,5]thieno[2,3-c]pyridine (1.5 g, 4.42 mmol), (3,5-dimethylphenyl)boronic acid (0.730 g, 4.87 mmol) and potassium carbonate (anh. powder, 1.53 g, 11.06 mmol) were suspended in dioxane (60 mL) and water (15 mL) and degassed with nitrogen for 15 minutes. Pd(PPh)₄ (0.256 g, 0.221 mmol) was added and the reaction mixture heated to 50° C. for 18 hours. The reaction mixture was cooled to RT, diluted with EtOAc (150 mL) and water (50 mL), the phases separated, the organics washed with water (50 mL), brine (50 mL) and concentrated in vacuo. The residue was purified on the CombiFlash (120 g silica column, eluted with 5-45% EtOAc in isohexane, dry loaded on silica) to afford a cream solid, 7-chloro-1-(3,5-dimethylphenyl)-8-(trifluoromethyl)benzo[4,5]thieno[2,3-c]pyridine (1.20 g, 69% yield).

To a 100 mL 3-neck round bottom flask was added 7-chloro-1-(3,5-dimethylphenyl)-8-(trifluoromethyl)benzo[4,5]thieno[2,3-c]pyridine (1.4 g, 3.57 mmol), (4-(3,3,3-trifluoro-2,2-dimethylpropyl)phenyl)boronic acid (0.961 g, 3.91 mmol), potassium phosphate tribasic (2.275 g, 10.72 mmol), dicyclohexyl(2′,6′-dimethoxy-[1,1′-biphenyl]-2-yl)phosphane (0.235 g, 0.572 mmol), dioxane (30 ml), and water (3 ml). Nitrogen was bubbled into the mixture for 10 mins. Pd₂(dba)₃ (0.131 g, 0.143 mmol) was added and the mixture was heated at 100° C. overnight under nitrogen. After reaction was cooled to RT, it was diluted with ethyl acetate and water, and extracted with ethyl acetate, and the organic extracts were evaporated to give a yellow solid, and purified on a silica gel column to give product 1.55 g.

1-(3,5-dimethylphenyl)-7-(4-(3,3,3-trifluoro-2,2-dimethylpropyl)phenyl)-8-(trifluoromethyl) benzo[4,5]thieno[2,3-c]pyridine (1.566 g, 2.81 mmol) was added to a solution of iridium chloride (0.45 g, 1.276 mmol). Nitrogen was bubbled into the mixture, the mixture was heated to 130° C. overnight under nitrogen. After reaction was cooled to RT, 3,7-diethylnonane-4,6-dione (0.677 g, 3.19 mmol), DMSO (100 ml), and potassium carbonate (0.441 g, 3.19 mmol) were added. The mixture was heated at 110° C. overnight under nitrogen. After reaction, the mixture was diluted with methanol, filtered off red colored solid. The solid was purified on a silica gel column to give product 1.4 g.

A solution of 1,8-dichlorobenzothiopheno[2,3-c]pyridine (4.0 g, 15.74 mmol), 3,5-Dimethylphenyl boronic acid (2.36 g, 15.74 mmol), Potassium carbonate (6.53 g, 47.22 mmol) dissolved in 1,4-dioxane (80 mL)/water (80 mL) was prepared. The mixture was degassed with nitrogen for 15 minutes. Then, tetrakis(triphenylphosphine)palladium(O) (0.91 g, 0.787 mmol) was added and the reaction was further degassed for 10 minutes. The mixture was stirred at 72° C. under nitrogen for 16 hours. The reaction mixture was filtered through Celite (diatomaceous earth) and then diluted with Et₂O (50 mL) and water (100 mL) and extracted three times with Et₂O. The organic phase were collected, combined, dried over magnesium sulfate, filtered and evaporated under reduce pressure. The residue was purified by silica gel column chromatography (70-30 Isohexane-EtOAc in gradient) to afford product as a yellow oil (2.45 g, 48% yield).

A solution of 8-chloro-1-(3,5-dimethylphenyl)benzothiopheno[2,3-c]pyridine (3 g, 9.26 mmol), Isobutylboronic acid (3.78 g, 37.06 mmol), Potassium Phosphate Tribasic (7.98 g, 37.06 mmol) were dissolved in toluene (80 mL)/water (15 mL). The mixture was degassed with nitrogen for 15 minutes. Then, dicyclohexyl(2′,6′-dimethoxy-[1,1′-biphenyl]-2-yl)phosphine (SPhos) (380 mg, 0.926 mmol) and Palladium (II) acetate (104 mg, 0.463 mmol) were added and the reaction was further degassed for 10 minutes. The mixture was stirred at 90° C. under nitrogen for 16 hours. The reaction mixture was filtered through Celite and the solution diluted with Et₂O (50 mL) and water (100 mL) and extracted three times with Et₂O. The organic phase was collected, combined, dried over magnesium sulfate, filtered and evaporated under reduce pressure. The residue was purified by silica gel column chromatography (85-15 Isohexane-EtOAc) to afford product as a yellow oil (2.8 g, 87% yield).

1-(3,5-dimethylphenyl)-8-isobutylbenzo[4,5]thieno[2,3-c]pyridine (1.122 g, 3.25 mmol) was added to a solution of iridium chloride (0.5 g, 1.418 mmol). Nitrogen was bubbled into the mixture and the reaction was heated at 100° overnight under nitrogen. The reaction mixture was directly used in next step without further purification. The product from the previous step, 3,7-diethylnonane-4,6-dione (0.753 g, 3.55 mmol), DMSO (150 ml) and potassium carbonate (0.490 g, 3.55 mmol) were added to a 50 ml round bottom flask. Nitrogen was bubbled into the mixture. The mixture was heated at 50° C. overnight under nitrogen. After reaction, the mixture was diluted with DCM, filtered through Celite, and washed DCM. After the solvent was removed, the residue was dissolved in DCM and purified on a silica gel column to give 0.71 g product.

Device Examples

All example devices were fabricated by high vacuum (<10⁻⁷ Torr) thermal evaporation. The anode electrode was 1,200 Å of indium tin oxide (ITO). The cathode consisted of 10 Å of Liq (8-hydroxyquinoline lithium) followed by 1,000 Å of Al. All devices were encapsulated with a glass lid sealed with an epoxy resin in a nitrogen glove box (<1 ppm of H₂O and O₂) immediately after fabrication, and a moisture getter was incorporated inside the package. The organic stack of the device examples consisted of sequentially, from the ITO surface, 100 Å of LG101 (purchased from LG Chem) as the hole injection layer (HIL); 400 Å of HTM as a hole transporting layer (HTL); 50 Å of EBM as a electron blocking layer (EBL); 400 Å of an emissive layer (EML) containing RH and 18% RH2 as red host and 3% of emitter, and 350 Å of Liq (8-hydroxyquinolinelithium) doped with 35% of ETM as the electron transporting layer (ETL). Table 1 shows the thickness of the device layers and materials.

TABLE 1 Device layer materials and thicknesses Thickness Layer Material [Å] Anode ITO 1,200 HIL LG101 100 HTL HTM 400 EBL EBM 50 EML RHL:RH2 18%: 400 Red emitter 3% ETL Liq: ETM 35% 350 EIL Liq 10 Cathode Al 1,000

The chemical structures of the device materials are shown below:

Upon fabrication, the devices were tested for EL and JVL. For this purpose, the sample was energized by the 2 channel Keysight B2902A SMU at a current density of 10 mA/cm² and measured by the Photo Research PR735 Spectroradiometer. Radiance (W/str/cm²) from 380 nm to 1080 nm, and total integrated photon count were collected. The devices were then placed under a large area silicon photodiode for the JVL sweep. The integrated photon count of the device at 10 mA/cm² is used to convert the photodiode current to photon count. The voltage was swept from 0 to a voltage equating to 200 mA/cm². The EQE of the devices were calculated using the total integrated photon count. LT95 is time for the luminescence decaying to 95% of the initial value measured at 80 mA/cm². All results are summarized in Table 2. Voltage, EQE, and LT95 of Device 1, containing the Inventive Example emitter, are reported as relative numbers normalized to the measured values of Device 2, containing the Comparative Example emitter.

TABLE 2 λ max At 10 mA/cm² Device Red emitter [nm] Voltage [V] EQE [%] LT95 [hr] Device 1 Inventive 618 1.02 1.03 1.79 Example Device 2 Comparative 595 1.00 1.00 1.00 Example

Table 2 summarizes the performance of the electroluminescence devices tested. Device 1 containing the Inventive Example emitter exhibited a saturated red color with λmax=618 nm. In addition, Device 1 exhibited higher EQE and much better device lifetime than Device 2. Thus, although both of the two red emitter compounds compared contained a L_(A) ligand with dibenzothiophene group, the device with Inventive Example exhibited better performance. These values were beyond any value that could be attributed to experimental error and the observed enhanced performance of Device 1 over Device 2 were significant and unexpected. In summary, the inventive materials can be used in organic electroluminescence device to improve overall device performance. 

What is claimed is:
 1. A compound comprising a first ligand L_(A) of Formula I

wherein: ring C is a 5-membered or 6-membered carbocyclic or heterocyclic ring; each of X¹ to X⁸ is independently C or N; one of X¹ to X⁴ is C and is connected to ring C, and one of X¹ to X⁴ is N and is coordinated to a metal M; Y is selected from the group consisting of O, S, Se, NR′, BR′, BR′R″, CR′R″, SiR′R″, GeR′R″, C═O, C═CRR′, and C═NR′; K is selected from the group consisting of a direct bond, O, and S; each of R^(A), R^(B), and R^(C) independently represents mono to the maximum allowable substitution, or no substitution; each R′, R″, R^(A), R^(B), and R^(C) is independently a hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, boryl, arylalkyl, alkoxy, aryloxy, amino, silyl, germyl, selenyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; at least one of R^(A) or R^(B) comprises an electron-withdrawing group; at least one of R^(B) is a cyclic group; L_(A) is coordinated to a metal M via the indicated dashed lines; metal M is selected from the group consisting of Os, Ir, Pd, Pt, Cu, Ag, and Au; L_(A) can be joined with other ligands to comprise a tridentate, tetradentate, pentadentate, and hexadentate ligand; and any two substituents can be joined or fused to form a ring.
 2. The compound of claim 1, wherein each R′, R″, R^(A), R^(B), and R^(C) is independently a hydrogen or a substituent selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile, isonitrile, sulfanyl, and combinations thereof.
 3. The compound of claim 1, wherein no R^(A), at least one R^(A), or exactly one R^(A) comprises an electron-withdrawing group; and/or wherein no R^(B) or at least one R^(B) comprises an electron-withdrawing group.
 4. The compound of claim 1, wherein the electron-withdrawing group is selected from the group consisting of F, CF₃, CN, COCH₃, CHO, COCF₃, COOMe, COOCF₃, NO₂, SF₃, SiF₃, PF₄, SF₅, OCF₃, SCF₃, SeCF₃, SOCF₃, SeOCF₃, SO₂F, SO₂CF₃, SeO₂CF₃, OSO₂CF₃, OSeO₂CF₃, OCN, SCN, SeCN, NC, ⁺N(R)₃, (R)₂CCN, (R)₂CCF₃, CNC(CF₃)₂,

wherein each R is independently a hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.
 5. The compound of claim 1, wherein the R^(B) attached to any or all of X⁵, X⁶, X⁷, and X⁸ is an electron-withdrawing group; and/or wherein the R^(A) attached to any or all of X¹, X², X³, and X⁴ is an electron-withdrawing group.
 6. The compound of claim 1, wherein at least one R^(B) is a pendant cyclic group; and/or wherein R^(B) attached to X⁵, X⁶, X⁷, or X⁸ is a pendant cyclic group; and/or wherein two R^(B) are joined or fused to form the cyclic group; and/or wherein R^(B) attached to X⁷ is a cyclic group and R^(B) attached to X⁸ is an electron-withdrawing group; and/or wherein the cyclic group comprises an electron-withdrawing group.
 7. The compound of claim 1, wherein ring C is a 5-membered, or 6-membered aryl or heteroaryl ring; and/or wherein two R^(C) are joined to form a ring fused to ring C; and/or wherein two R^(C) are joined to form a polycyclic fused ring structure.
 8. The compound of claim 1, wherein the ligand L_(A) is selected from the group consisting of:


9. The compound of claim 1, wherein the ligand L_(A) is selected from the group consisting of:

wherein Y² is selected from the group consisting of O, S, Se, NR^(Y′), BR^(Y′), BR^(Y′)R^(Y″), CR^(Y′)R^(Y″), SiR^(Y′)R^(Y″), GeR^(Y′)R^(Y″), C═O, C═CR^(Y′)R^(Y″), and C═NR^(Y′), and wherein each of R^(Y′) and R^(Y) is independently a hydrogen or a substituent selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile, isonitrile, sulfanyl, and combinations thereof.
 10. The compound of claim 1, wherein the ligand L_(A) is selected from the group consisting of: L_(Ai-m-X), where i is an integer from 1 to 2964, m is an integer from 1 to 52, and X is an integer from 1 to 4, where X=1 represents O, X=2 represents S, X=3 represents NCH₃, and X=4 represents Se; wherein each of L_(Ai-i-X) to L_(Ai-52-X) has a structure defined as follows:

wherein, for each i from 1 to 2964, R^(E) and G are defined as follows: i R^(E) G i R^(E) G i R^(E) G i R^(E) G 1 R¹ G¹ 2 R¹ G² 3 R¹ G³ 4 R¹ G⁴ 5 R² G¹ 6 R² G² 7 R² G³ 8 R² G⁴ 9 R³ G¹ 10 R³ G² 11 R³ G³ 12 R³ G⁴ 13 R⁴ G¹ 14 R⁴ G² 15 R⁴ G³ 16 R⁴ G⁴ 17 R⁵ G¹ 18 R⁵ G² 19 R⁵ G³ 20 R⁵ G⁴ 21 R⁶ G¹ 22 R⁶ G² 23 R⁶ G³ 24 R⁶ G⁴ 25 R⁷ G¹ 26 R⁷ G² 27 R⁷ G³ 28 R⁷ G⁴ 29 R⁸ G¹ 30 R⁸ G² 31 R⁸ G³ 32 R⁸ G⁴ 33 R⁹ G¹ 34 R⁹ G² 35 R⁹ G³ 36 R⁹ G⁴ 37 R¹⁰ G¹ 38 R¹⁰ G² 39 R¹⁰ G³ 40 R¹⁰ G⁴ 41 R¹¹ G¹ 42 R¹¹ G² 43 R¹¹ G³ 44 R¹¹ G⁴ 45 R¹² G¹ 46 R¹² G² 47 R¹² G³ 48 R¹² G⁴ 49 R¹³ G¹ 50 R¹³ G² 51 R¹³ G³ 52 R¹³ G⁴ 53 R¹⁴ G¹ 54 R¹⁴ G² 55 R¹⁴ G³ 56 R¹⁴ G⁴ 57 R¹⁵ G¹ 58 R¹⁵ G² 59 R¹⁵ G³ 60 R¹⁵ G⁴ 61 R¹⁶ G¹ 62 R¹⁶ G² 63 R¹⁶ G³ 64 R¹⁶ G⁴ 65 R¹⁷ G¹ 66 R¹⁷ G² 67 R¹⁷ G³ 68 R¹⁷ G⁴ 69 R¹⁸ G¹ 70 R¹⁸ G² 71 R¹⁸ G³ 72 R¹⁸ G⁴ 73 R¹⁹ G¹ 74 R¹⁹ G² 75 R¹⁹ G³ 76 R¹⁹ G⁴ 77 R²⁰ G¹ 78 R²⁰ G² 79 R²⁰ G³ 80 R²⁰ G⁴ 81 R²¹ G¹ 82 R²¹ G² 83 R²¹ G³ 84 R²¹ G⁴ 85 R²² G¹ 86 R²² G² 87 R²² G³ 88 R²² G⁴ 89 R²³ G¹ 90 R²³ G² 91 R²³ G³ 92 R²³ G⁴ 93 R²⁴ G¹ 94 R²⁴ G² 95 R²⁴ G³ 96 R²⁴ G⁴ 97 R²⁵ G¹ 98 R²⁵ G² 99 R²⁵ G³ 100 R²⁵ G⁴ 101 R²⁶ G¹ 102 R²⁶ G² 103 R²⁶ G³ 104 R²⁶ G⁴ 105 R²⁷ G¹ 106 R²⁷ G² 107 R²⁷ G³ 108 R²⁷ G⁴ 109 R²⁸ G¹ 110 R²⁸ G² 111 R²⁸ G³ 112 R²⁸ G⁴ 113 R²⁹ G¹ 114 R²⁹ G² 115 R²⁹ G³ 116 R²⁹ G⁴ 117 R³⁰ G¹ 118 R³⁰ G² 119 R³⁰ G³ 120 R³⁰ G⁴ 121 R³¹ G¹ 122 R³¹ G² 123 R³¹ G³ 124 R³¹ G⁴ 125 R³² G¹ 126 R³² G² 127 R³² G³ 128 R³² G⁴ 129 R³³ G¹ 130 R³³ G² 131 R³³ G³ 132 R³³ G⁴ 133 R³⁴ G¹ 134 R³⁴ G² 135 R³⁴ G³ 136 R³⁴ G⁴ 137 R³⁵ G¹ 138 R³⁵ G² 139 R³⁵ G³ 140 R³⁵ G⁴ 141 R³⁶ G¹ 142 R³⁶ G² 143 R³⁶ G³ 144 R³⁶ G⁴ 145 R³⁷ G¹ 146 R³⁷ G² 147 R³⁷ G³ 148 R³⁷ G⁴ 149 R³⁸ G¹ 150 R³⁸ G² 151 R³⁸ G³ 152 R³⁸ G⁴ 153 R³⁹ G¹ 154 R³⁹ G² 155 R³⁹ G³ 156 R³⁹ G⁴ 157 R⁴⁰ G¹ 158 R⁴⁰ G² 159 R⁴⁰ G³ 160 R⁴⁰ G⁴ 161 R⁴¹ G¹ 162 R⁴¹ G² 163 R⁴¹ G³ 164 R⁴¹ G⁴ 165 R⁴² G¹ 166 R⁴² G² 167 R⁴² G³ 168 R⁴² G⁴ 169 R⁴³ G¹ 170 R⁴³ G² 171 R⁴³ G³ 172 R⁴³ G⁴ 173 R⁴⁴ G¹ 174 R⁴⁴ G² 175 R⁴⁴ G³ 176 R⁴⁴ G⁴ 177 R⁴⁵ G¹ 178 R⁴⁵ G² 179 R⁴⁵ G³ 180 R⁴⁵ G⁴ 181 R⁴⁶ G¹ 182 R⁴⁶ G² 183 R⁴⁶ G³ 184 R⁴⁶ G⁴ 185 R⁴⁷ G¹ 186 R⁴⁷ G² 187 R⁴⁷ G³ 188 R⁴⁷ G⁴ 189 R⁴⁸ G¹ 190 R⁴⁸ G² 191 R⁴⁸ G³ 192 R⁴⁸ G⁴ 193 R⁴⁹ G¹ 194 R⁴⁹ G² 195 R⁴⁹ G³ 196 R⁴⁹ G⁴ 197 R⁵⁰ G¹ 198 R⁵⁰ G² 199 R⁵⁰ G³ 200 R⁵⁰ G⁴ 201 R⁵¹ G¹ 202 R⁵¹ G² 203 R⁵¹ G³ 204 R⁵¹ G⁴ 205 R⁵² G¹ 206 R⁵² G² 207 R⁵² G³ 208 R⁵² G⁴ 209 R⁵³ G¹ 210 R⁵³ G² 211 R⁵³ G³ 212 R⁵³ G⁴ 213 R⁵⁴ G¹ 214 R⁵⁴ G² 215 R⁵⁴ G³ 216 R⁵⁴ G⁴ 217 R⁵⁵ G¹ 218 R⁵⁵ G² 219 R⁵⁵ G³ 220 R⁵⁵ G⁴ 221 R⁵⁶ G¹ 222 R⁵⁶ G² 223 R⁵⁶ G³ 224 R⁵⁶ G⁴ 225 R⁵⁷ G¹ 226 R⁵⁷ G² 227 R⁵⁷ G³ 228 R⁵⁷ G⁴ 229 R¹ G⁵ 230 R¹ G⁶ 231 R¹ G⁷ 232 R¹ G⁸ 233 R² G⁵ 234 R² G⁶ 235 R² G⁷ 236 R² G⁸ 237 R³ G⁵ 238 R³ G⁶ 239 R³ G⁷ 240 R³ G⁸ 241 R⁴ G⁵ 242 R⁴ G⁶ 243 R⁴ G⁷ 244 R⁴ G⁸ 245 R⁵ G⁵ 246 R⁵ G⁶ 247 R⁵ G⁷ 248 R⁵ G⁸ 249 R⁶ G⁵ 250 R⁶ G⁶ 251 R⁶ G⁷ 252 R⁶ G⁸ 253 R⁷ G⁵ 254 R⁷ G⁶ 255 R⁷ G⁷ 256 R⁷ G⁸ 257 R⁸ G⁵ 258 R⁸ G⁶ 259 R⁸ G⁷ 260 R⁸ G⁸ 261 R⁹ G⁵ 262 R⁹ G⁶ 263 R⁹ G⁷ 264 R⁹ G⁸ 265 R¹⁰ G⁵ 266 R¹⁰ G⁶ 267 R¹⁰ G⁷ 268 R¹⁰ G⁸ 269 R¹¹ G⁵ 270 R¹¹ G⁶ 271 R¹¹ G⁷ 272 R¹¹ G⁸ 273 R¹² G⁵ 274 R¹² G⁶ 275 R¹² G⁷ 276 R¹² G⁸ 277 R¹³ G⁵ 278 R¹³ G⁶ 279 R¹³ G⁷ 280 R¹³ G⁸ 281 R¹⁴ G⁵ 282 R¹⁴ G⁶ 283 R¹⁴ G⁷ 284 R¹⁴ G⁸ 285 R¹⁵ G⁵ 286 R¹⁵ G⁶ 287 R¹⁵ G⁷ 288 R¹⁵ G⁸ 289 R¹⁶ G⁵ 290 R¹⁶ G⁶ 291 R¹⁶ G⁷ 292 R¹⁶ G⁸ 293 R¹⁷ G⁵ 294 R¹⁷ G⁶ 295 R¹⁷ G⁷ 296 R¹⁷ G⁸ 297 R¹⁸ G⁵ 298 R¹⁸ G⁶ 299 R¹⁸ G⁷ 300 R¹⁸ G⁸ 301 R¹⁹ G⁵ 302 R¹⁹ G⁶ 303 R¹⁹ G⁷ 304 R¹⁹ G⁸ 305 R²⁰ G⁵ 306 R²⁰ G⁶ 307 R²⁰ G⁷ 308 R²⁰ G⁸ 309 R²¹ G⁵ 310 R²¹ G⁶ 311 R²¹ G⁷ 312 R²¹ G⁸ 313 R²² G⁵ 314 R²² G⁶ 315 R²² G⁷ 316 R²² G⁸ 317 R²³ G⁵ 318 R²³ G⁶ 319 R²³ G⁷ 320 R²³ G⁸ 321 R²⁴ G⁵ 322 R²⁴ G⁶ 323 R²⁴ G⁷ 324 R²⁴ G⁸ 325 R²⁵ G⁵ 326 R²⁵ G⁶ 327 R²⁵ G⁷ 328 R²⁵ G⁸ 329 R²⁶ G⁵ 330 R²⁶ G⁶ 331 R²⁶ G⁷ 332 R²⁶ G⁸ 333 R²⁷ G⁵ 334 R²⁷ G⁶ 335 R²⁷ G⁷ 336 R²⁷ G⁸ 337 R²⁸ G⁵ 338 R²⁸ G⁶ 339 R²⁸ G⁷ 340 R²⁸ G⁸ 341 R²⁹ G⁵ 342 R²⁹ G⁶ 343 R²⁹ G⁷ 344 R²⁹ G⁸ 345 R³⁰ G⁵ 346 R³⁰ G⁶ 347 R³⁰ G⁷ 348 R³⁰ G⁸ 349 R³¹ G⁵ 350 R³¹ G⁶ 351 R³¹ G⁷ 352 R³¹ G⁸ 353 R³² G⁵ 354 R³² G⁶ 355 R³² G⁷ 356 R³² G⁸ 357 R³³ G⁵ 358 R³³ G⁶ 359 R³³ G⁷ 360 R³³ G⁸ 361 R³⁴ G⁵ 362 R³⁴ G⁶ 363 R³⁴ G⁷ 364 R³⁴ G⁸ 365 R³⁵ G⁵ 366 R³⁵ G⁶ 367 R³⁵ G⁷ 368 R³⁵ G⁸ 369 R³⁶ G⁵ 370 R³⁶ G⁶ 371 R³⁶ G⁷ 372 R³⁶ G⁸ 373 R³⁷ G⁵ 374 R³⁷ G⁶ 375 R³⁷ G⁷ 376 R³⁷ G⁸ 377 R³⁸ G⁵ 378 R³⁸ G⁶ 379 R³⁸ G⁷ 380 R³⁸ G⁸ 381 R³⁹ G⁵ 382 R³⁹ G⁶ 383 R³⁹ G⁷ 384 R³⁹ G⁸ 385 R⁴⁰ G⁵ 386 R⁴⁰ G⁶ 387 R⁴⁰ G⁷ 388 R⁴⁰ G⁸ 389 R⁴¹ G⁵ 390 R⁴¹ G⁶ 391 R⁴¹ G⁷ 392 R⁴¹ G⁸ 393 R⁴² G⁵ 394 R⁴² G⁶ 395 R⁴² G⁷ 396 R⁴² G⁸ 397 R⁴³ G⁵ 398 R⁴³ G⁶ 399 R⁴³ G⁷ 400 R⁴³ G⁸ 401 R⁴⁴ G⁵ 402 R⁴⁴ G⁶ 403 R⁴⁴ G⁷ 404 R⁴⁴ G⁸ 405 R⁴⁵ G⁵ 406 R⁴⁵ G⁶ 407 R⁴⁵ G⁷ 408 R⁴⁵ G⁸ 409 R⁴⁶ G⁵ 410 R⁴⁶ G⁶ 411 R⁴⁶ G⁷ 412 R⁴⁶ G⁸ 413 R⁴⁷ G⁵ 414 R⁴⁷ G⁶ 415 R⁴⁷ G⁷ 416 R⁴⁷ G⁸ 417 R⁴⁸ G⁵ 418 R⁴⁸ G⁶ 419 R⁴⁸ G⁷ 420 R⁴⁸ G⁸ 421 R⁴⁹ G⁵ 422 R⁴⁹ G⁶ 423 R⁴⁹ G⁷ 424 R⁴⁹ G⁸ 425 R⁵⁰ G⁵ 426 R⁵⁰ G⁶ 427 R⁵⁰ G⁷ 428 R⁵⁰ G⁸ 429 R⁵¹ G⁵ 430 R⁵¹ G⁶ 431 R⁵¹ G⁷ 432 R⁵¹ G⁸ 433 R⁵² G⁵ 434 R⁵² G⁶ 435 R⁵² G⁷ 436 R⁵² G⁸ 437 R⁵³ G⁵ 438 R⁵³ G⁶ 439 R⁵³ G⁷ 440 R⁵³ G⁸ 441 R⁵⁴ G⁵ 442 R⁵⁴ G⁶ 443 R⁵⁴ G⁷ 444 R⁵⁴ G⁸ 445 R⁵⁵ G⁵ 446 R⁵⁵ G⁶ 447 R⁵⁵ G⁷ 448 R⁵⁵ G⁸ 449 R⁵⁶ G⁵ 450 R⁵⁶ G⁶ 451 R⁵⁶ G⁷ 452 R⁵⁶ G⁸ 453 R⁵⁷ G⁵ 454 R⁵⁷ G⁶ 455 R⁵⁷ G⁷ 456 R⁵⁷ G⁸ 457 R¹ G⁹ 458 R¹ G¹⁰ 459 R¹ G¹¹ 460 R¹ G¹² 461 R² G⁹ 462 R² G¹⁰ 463 R² G¹¹ 464 R² G¹² 465 R³ G⁹ 466 R³ G¹⁰ 467 R³ G¹¹ 468 R³ G¹² 469 R⁴ G⁹ 470 R⁴ G¹⁰ 471 R⁴ G¹¹ 472 R⁴ G¹² 473 R⁵ G⁹ 474 R⁵ G¹⁰ 475 R⁵ G¹¹ 476 R⁵ G¹² 477 R⁶ G⁹ 478 R⁶ G¹⁰ 479 R⁶ G¹¹ 480 R⁶ G¹² 481 R⁷ G⁹ 482 R⁷ G¹⁰ 483 R⁷ G¹¹ 484 R⁷ G¹² 485 R⁸ G⁹ 486 R⁸ G¹⁰ 487 R⁸ G¹¹ 488 R⁸ G¹² 489 R⁹ G⁹ 490 R⁹ G¹⁰ 491 R⁹ G¹¹ 492 R⁹ G¹² 493 R¹⁰ G⁹ 494 R¹⁰ G¹⁰ 495 R¹⁰ G¹¹ 496 R¹⁰ G¹² 497 R¹¹ G⁹ 498 R¹¹ G¹⁰ 499 R¹¹ G¹¹ 500 R¹¹ G¹² 501 R¹² G⁹ 502 R¹² G¹⁰ 503 R¹² G¹¹ 504 R¹² G¹² 505 R¹³ G⁹ 506 R¹³ G¹⁰ 507 R¹³ G¹¹ 508 R¹³ G¹² 509 R¹⁴ G⁹ 510 R¹⁴ G¹⁰ 511 R¹⁴ G¹¹ 512 R¹⁴ G¹² 513 R¹⁵ G⁹ 514 R¹⁵ G¹⁰ 515 R¹⁵ G¹¹ 516 R¹⁵ G¹² 517 R¹⁶ G⁹ 518 R¹⁶ G¹⁰ 519 R¹⁶ G¹¹ 520 R¹⁶ G¹² 521 R¹⁷ G⁹ 522 R¹⁷ G¹⁰ 523 R¹⁷ G¹¹ 524 R¹⁷ G¹² 525 R¹⁸ G⁹ 526 R¹⁸ G¹⁰ 527 R¹⁸ G¹¹ 528 R¹⁸ G¹² 529 R¹⁹ G⁹ 530 R¹⁹ G¹⁰ 531 R¹⁹ G¹¹ 532 R¹⁹ G¹² 533 R²⁰ G⁹ 534 R²⁰ G¹⁰ 535 R²⁰ G¹¹ 536 R²⁰ G¹² 537 R²¹ G⁹ 538 R²¹ G¹⁰ 539 R²¹ G¹¹ 540 R²¹ G¹² 541 R²² G⁹ 542 R²² G¹⁰ 543 R²² G¹¹ 544 R²² G¹² 545 R²³ G⁹ 546 R²³ G¹⁰ 547 R²³ G¹¹ 548 R²³ G¹² 549 R²⁴ G⁹ 550 R²⁴ G¹⁰ 551 R²⁴ G¹¹ 552 R²⁴ G¹² 553 R²⁵ G⁹ 554 R²⁵ G¹⁰ 555 R²⁵ G¹¹ 556 R²⁵ G¹² 557 R²⁶ G⁹ 558 R²⁶ G¹⁰ 559 R²⁶ G¹¹ 560 R²⁶ G¹² 561 R²⁷ G⁹ 562 R²⁷ G¹⁰ 563 R²⁷ G¹¹ 564 R²⁷ G¹² 565 R²⁸ G⁹ 566 R²⁸ G¹⁰ 567 R²⁸ G¹¹ 568 R²⁸ G¹² 569 R²⁹ G⁹ 570 R²⁹ G¹⁰ 571 R²⁹ G¹¹ 572 R²⁹ G¹² 573 R³⁰ G⁹ 574 R³⁰ G¹⁰ 575 R³⁰ G¹¹ 576 R³⁰ G¹² 577 R³¹ G⁹ 578 R³¹ G¹⁰ 579 R³¹ G¹¹ 580 R³¹ G¹² 581 R³² G⁹ 582 R³² G¹⁰ 583 R³² G¹¹ 584 R³² G¹² 585 R³³ G⁹ 586 R³³ G¹⁰ 587 R³³ G¹¹ 588 R³³ G¹² 589 R³⁴ G⁹ 590 R³⁴ G¹⁰ 591 R³⁴ G¹¹ 592 R³⁴ G¹² 593 R³⁵ G⁹ 594 R³⁵ G¹⁰ 595 R³⁵ G¹¹ 596 R³⁵ G¹² 597 R³⁶ G⁹ 598 R³⁶ G¹⁰ 599 R³⁶ G¹¹ 600 R³⁶ G¹² 601 R³⁷ G⁹ 602 R³⁷ G¹⁰ 603 R³⁷ G¹¹ 604 R³⁷ G¹² 605 R³⁸ G⁹ 606 R³⁸ G¹⁰ 607 R³⁸ G¹¹ 608 R³⁸ G¹² 609 R³⁹ G⁹ 610 R³⁹ G¹⁰ 611 R³⁹ G¹¹ 612 R³⁹ G¹² 613 R⁴⁰ G⁹ 614 R⁴⁰ G¹⁰ 615 R⁴⁰ G¹¹ 616 R⁴⁰ G¹² 617 R⁴¹ G⁹ 618 R⁴¹ G¹⁰ 619 R⁴¹ G¹¹ 620 R⁴¹ G¹² 621 R⁴² G⁹ 622 R⁴² G¹⁰ 623 R⁴² G¹¹ 624 R⁴² G¹² 625 R⁴³ G⁹ 626 R⁴³ G¹⁰ 627 R⁴³ G¹¹ 628 R⁴³ G¹² 629 R⁴⁴ G⁹ 630 R⁴⁴ G¹⁰ 631 R⁴⁴ G¹¹ 632 R⁴⁴ G¹² 633 R⁴⁵ G⁹ 634 R⁴⁵ G¹⁰ 635 R⁴⁵ G¹¹ 636 R⁴⁵ G¹² 637 R⁴⁶ G⁹ 638 R⁴⁶ G¹⁰ 639 R⁴⁶ G¹¹ 640 R⁴⁶ G¹² 641 R⁴⁷ G⁹ 642 R⁴⁷ G¹⁰ 643 R⁴⁷ G¹¹ 644 R⁴⁷ G¹² 645 R⁴⁸ G⁹ 646 R⁴⁸ G¹⁰ 647 R⁴⁸ G¹¹ 648 R⁴⁸ G¹² 649 R⁴⁹ G⁹ 650 R⁴⁹ G¹⁰ 651 R⁴⁹ G¹¹ 652 R⁴⁹ G¹² 653 R⁵⁰ G⁹ 654 R⁵⁰ G¹⁰ 655 R⁵⁰ G¹¹ 656 R⁵⁰ G¹² 657 R⁵¹ G⁹ 658 R⁵¹ G¹⁰ 659 R⁵¹ G¹¹ 660 R⁵¹ G¹² 661 R⁵² G⁹ 662 R⁵² G¹⁰ 663 R⁵² G¹¹ 664 R⁵² G¹² 665 R⁵³ G⁹ 666 R⁵³ G¹⁰ 667 R⁵³ G¹¹ 668 R⁵³ G¹² 669 R⁵⁴ G⁹ 670 R⁵⁴ G¹⁰ 671 R⁵⁴ G¹¹ 672 R⁵⁴ G¹² 673 R⁵⁵ G⁹ 674 R⁵⁵ G¹⁰ 675 R⁵⁵ G¹¹ 676 R⁵⁵ G¹² 677 R⁵⁶ G⁹ 678 R⁵⁶ G¹⁰ 679 R⁵⁶ G¹¹ 680 R⁵⁶ G¹² 681 R⁵⁷ G⁹ 682 R⁵⁷ G¹⁰ 683 R⁵⁷ G¹¹ 684 R⁵⁷ G¹² 685 R¹ G¹³ 686 R¹ G¹⁴ 687 R¹ G¹⁵ 688 R¹ G¹⁶ 689 R² G¹³ 690 R² G¹⁴ 691 R² G¹⁵ 692 R² G¹⁶ 693 R³ G¹³ 694 R³ G¹⁴ 695 R³ G¹⁵ 696 R³ G¹⁶ 697 R⁴ G¹³ 698 R⁴ G¹⁴ 699 R⁴ G¹⁵ 700 R⁴ G¹⁶ 701 R⁵ G¹³ 702 R⁵ G¹⁴ 703 R⁵ G¹⁵ 704 R⁵ G¹⁶ 705 R⁶ G¹³ 706 R⁶ G¹⁴ 707 R⁶ G¹⁵ 708 R⁶ G¹⁶ 709 R⁷ G¹³ 710 R⁷ G¹⁴ 711 R⁷ G¹⁵ 712 R⁷ G¹⁶ 713 R⁸ G¹³ 714 R⁸ G¹⁴ 715 R⁸ G¹⁵ 716 R⁸ G¹⁶ 717 R⁹ G¹³ 718 R⁹ G¹⁴ 719 R⁹ G¹⁵ 720 R⁹ G¹⁶ 721 R¹⁰ G¹³ 722 R¹⁰ G¹⁴ 723 R¹⁰ G¹⁵ 724 R¹⁰ G¹⁶ 725 R¹¹ G¹³ 726 R¹¹ G¹⁴ 727 R¹¹ G¹⁵ 728 R¹¹ G¹⁶ 729 R¹² G¹³ 730 R¹² G¹⁴ 731 R¹² G¹⁵ 732 R¹² G¹⁶ 733 R¹³ G¹³ 734 R¹³ G¹⁴ 735 R¹³ G¹⁵ 736 R¹³ G¹⁶ 737 R¹⁴ G¹³ 738 R¹⁴ G¹⁴ 739 R¹⁴ G¹⁵ 740 R¹⁴ G¹⁶ 741 R¹⁵ G¹³ 742 R¹⁵ G¹⁴ 743 R¹⁵ G¹⁵ 744 R¹⁵ G¹⁶ 745 R¹⁶ G¹³ 746 R¹⁶ G¹⁴ 747 R¹⁶ G¹⁵ 748 R¹⁶ G¹⁶ 749 R¹⁷ G¹³ 750 R¹⁷ G¹⁴ 751 R¹⁷ G¹⁵ 752 R¹⁷ G¹⁶ 753 R¹⁸ G¹³ 754 R¹⁸ G¹⁴ 755 R¹⁸ G¹⁵ 756 R¹⁸ G¹⁶ 757 R¹⁹ G¹³ 758 R¹⁹ G¹⁴ 759 R¹⁹ G¹⁵ 760 R¹⁹ G¹⁶ 761 R²⁰ G¹³ 762 R²⁰ G¹⁴ 763 R²⁰ G¹⁵ 764 R²⁰ G¹⁶ 765 R²¹ G¹³ 766 R²¹ G¹⁴ 767 R²¹ G¹⁵ 768 R²¹ G¹⁶ 769 R²² G¹³ 770 R²² G¹⁴ 771 R²² G¹⁵ 772 R²² G¹⁶ 773 R²³ G¹³ 774 R²³ G¹⁴ 775 R²³ G¹⁵ 776 R²³ G¹⁶ 777 R²⁴ G¹³ 778 R²⁴ G¹⁴ 779 R²⁴ G¹⁵ 780 R²⁴ G¹⁶ 781 R²⁵ G¹³ 782 R²⁵ G¹⁴ 783 R²⁵ G¹⁵ 784 R²⁵ G¹⁶ 785 R²⁶ G¹³ 786 R²⁶ G¹⁴ 787 R²⁶ G¹⁵ 788 R²⁶ G¹⁶ 789 R²⁷ G¹³ 790 R²⁷ G¹⁴ 791 R²⁷ G¹⁵ 792 R²⁷ G¹⁶ 793 R²⁸ G¹³ 794 R²⁸ G¹⁴ 795 R²⁸ G¹⁵ 796 R²⁸ G¹⁶ 797 R²⁹ G¹³ 798 R²⁹ G¹⁴ 799 R²⁹ G¹⁵ 800 R²⁹ G¹⁶ 801 R³⁰ G¹³ 802 R³⁰ G¹⁴ 803 R³⁰ G¹⁵ 804 R³⁰ G¹⁶ 805 R³¹ G¹³ 806 R³¹ G¹⁴ 807 R³¹ G¹⁵ 808 R³¹ G¹⁶ 809 R³² G¹³ 810 R³² G¹⁴ 811 R³² G¹⁵ 812 R³² G¹⁶ 813 R³³ G¹³ 814 R³³ G¹⁴ 815 R³³ G¹⁵ 816 R³³ G¹⁶ 817 R³⁴ G¹³ 818 R³⁴ G¹⁴ 819 R³⁴ G¹⁵ 820 R³⁴ G¹⁶ 821 R³⁵ G¹³ 822 R³⁵ G¹⁴ 823 R³⁵ G¹⁵ 824 R³⁵ G¹⁶ 825 R³⁶ G¹³ 826 R³⁶ G¹⁴ 827 R³⁶ G¹⁵ 828 R³⁶ G¹⁶ 829 R³⁷ G¹³ 830 R³⁷ G¹⁴ 831 R³⁷ G¹⁵ 832 R³⁷ G¹⁶ 833 R³⁸ G¹³ 834 R³⁸ G¹⁴ 835 R³⁸ G¹⁵ 836 R³⁸ G¹⁶ 837 R³⁹ G¹³ 838 R³⁹ G¹⁴ 839 R³⁹ G¹⁵ 840 R³⁹ G¹⁶ 841 R⁴⁰ G¹³ 842 R⁴⁰ G¹⁴ 843 R⁴⁰ G¹⁵ 844 R⁴⁰ G¹⁶ 845 R⁴¹ G¹³ 846 R⁴¹ G¹⁴ 847 R⁴¹ G¹⁵ 848 R⁴¹ G¹⁶ 849 R⁴² G¹³ 850 R⁴² G¹⁴ 851 R⁴² G¹⁵ 852 R⁴² G¹⁶ 853 R⁴³ G¹³ 854 R⁴³ G¹⁴ 855 R⁴³ G¹⁵ 856 R⁴³ G¹⁶ 857 R⁴⁴ G¹³ 858 R⁴⁴ G¹⁴ 859 R⁴⁴ G¹⁵ 860 R⁴⁴ G¹⁶ 861 R⁴⁵ G¹³ 862 R⁴⁵ G¹⁴ 863 R⁴⁵ G¹⁵ 864 R⁴⁵ G¹⁶ 865 R⁴⁶ G¹³ 866 R⁴⁶ G¹⁴ 867 R⁴⁶ G¹⁵ 868 R⁴⁶ G¹⁶ 869 R⁴⁷ G¹³ 870 R⁴⁷ G¹⁴ 871 R⁴⁷ G¹⁵ 872 R⁴⁷ G¹⁶ 873 R⁴⁸ G¹³ 874 R⁴⁸ G¹⁴ 875 R⁴⁸ G¹⁵ 876 R⁴⁸ G¹⁶ 877 R⁴⁹ G¹³ 878 R⁴⁹ G¹⁴ 879 R⁴⁹ G¹⁵ 880 R⁴⁹ G¹⁶ 881 R⁵⁰ G¹³ 882 R⁵⁰ G¹⁴ 883 R⁵⁰ G¹⁵ 884 R⁵⁰ G¹⁶ 885 R⁵¹ G¹³ 886 R⁵¹ G¹⁴ 887 R⁵¹ G¹⁵ 888 R⁵¹ G¹⁶ 889 R⁵² G¹³ 890 R⁵² G¹⁴ 891 R⁵² G¹⁵ 892 R⁵² G¹⁶ 893 R⁵³ G¹³ 894 R⁵³ G¹⁴ 895 R⁵³ G¹⁵ 896 R⁵³ G¹⁶ 897 R⁵⁴ G¹³ 898 R⁵⁴ G¹⁴ 899 R⁵⁴ G¹⁵ 900 R⁵⁴ G¹⁶ 901 R⁵⁵ G¹³ 902 R⁵⁵ G¹⁴ 903 R⁵⁵ G¹⁵ 904 R⁵⁵ G¹⁶ 905 R⁵⁶ G¹³ 906 R⁵⁶ G¹⁴ 907 R⁵⁶ G¹⁵ 908 R⁵⁶ G¹⁶ 909 R⁵⁷ G¹³ 910 R⁵⁷ G¹⁴ 911 R⁵⁷ G¹⁵ 912 R⁵⁷ G¹⁶ 913 R¹ G¹⁷ 914 R¹ G¹⁸ 915 R¹ G¹⁹ 916 R¹ G²⁰ 917 R² G¹⁷ 918 R² G¹⁸ 919 R² G¹⁹ 920 R² G²⁰ 921 R³ G¹⁷ 922 R³ G¹⁸ 923 R³ G¹⁹ 924 R³ G²⁰ 925 R⁴ G¹⁷ 926 R⁴ G¹⁸ 927 R⁴ G¹⁹ 928 R⁴ G²⁰ 929 R⁵ G¹⁷ 930 R⁵ G¹⁸ 931 R⁵ G¹⁹ 932 R⁵ G²⁰ 933 R⁶ G¹⁷ 934 R⁶ G¹⁸ 935 R⁶ G¹⁹ 936 R⁶ G²⁰ 937 R⁷ G¹⁷ 938 R⁷ G¹⁸ 939 R⁷ G¹⁹ 940 R⁷ G²⁰ 941 R⁸ G¹⁷ 942 R⁸ G¹⁸ 943 R⁸ G¹⁹ 944 R⁸ G²⁰ 945 R⁹ G¹⁷ 946 R⁹ G¹⁸ 947 R⁹ G¹⁹ 948 R⁹ G²⁰ 949 R¹⁰ G¹⁷ 950 R¹⁰ G¹⁸ 951 R¹⁰ G¹⁹ 952 R¹⁰ G²⁰ 953 R¹¹ G¹⁷ 954 R¹¹ G¹⁸ 955 R¹¹ G¹⁹ 956 R¹¹ G²⁰ 957 R¹² G¹⁷ 958 R¹² G¹⁸ 959 R¹² G¹⁹ 960 R¹² G²⁰ 961 R¹³ G¹⁷ 962 R¹³ G¹⁸ 963 R¹³ G¹⁹ 964 R¹³ G²⁰ 965 R¹⁴ G¹⁷ 966 R¹⁴ G¹⁸ 967 R¹⁴ G¹⁹ 968 R¹⁴ G²⁰ 969 R¹⁵ G¹⁷ 970 R¹⁵ G¹⁸ 971 R¹⁵ G¹⁹ 972 R¹⁵ G²⁰ 973 R¹⁶ G¹⁷ 974 R¹⁶ G¹⁸ 975 R¹⁶ G¹⁹ 976 R¹⁶ G²⁰ 977 R¹⁷ G¹⁷ 978 R¹⁷ G¹⁸ 979 R¹⁷ G¹⁹ 980 R¹⁷ G²⁰ 981 R¹⁸ G¹⁷ 982 R¹⁸ G¹⁸ 983 R¹⁸ G¹⁹ 984 R¹⁸ G²⁰ 985 R¹⁹ G¹⁷ 986 R¹⁹ G¹⁸ 987 R¹⁹ G¹⁹ 988 R¹⁹ G²⁰ 989 R²⁰ G¹⁷ 990 R²⁰ G¹⁸ 991 R²⁰ G¹⁹ 992 R²⁰ G²⁰ 993 R²¹ G¹⁷ 994 R²¹ G¹⁸ 995 R²¹ G¹⁹ 996 R²¹ G²⁰ 997 R²² G¹⁷ 998 R²² G¹⁸ 999 R²² G¹⁹ 1000 R²² G²⁰ 1001 R²³ G¹⁷ 1002 R²³ G¹⁸ 1003 R²³ G¹⁹ 1004 R²³ G²⁰ 1005 R²⁴ G¹⁷ 1006 R²⁴ G¹⁸ 1007 R²⁴ G¹⁹ 1008 R²⁴ G²⁰ 1009 R²⁵ G¹⁷ 1010 R²⁵ G¹⁸ 1011 R²⁵ G¹⁹ 1012 R²⁵ G²⁰ 1013 R²⁶ G¹⁷ 1014 R²⁶ G¹⁸ 1015 R²⁶ G¹⁹ 1016 R²⁶ G²⁰ 1017 R²⁷ G¹⁷ 1018 R²⁷ G¹⁸ 1019 R²⁷ G¹⁹ 1020 R²⁷ G²⁰ 1021 R²⁸ G¹⁷ 1022 R²⁸ G¹⁸ 1023 R²⁸ G¹⁹ 1024 R²⁸ G²⁰ 1025 R²⁹ G¹⁷ 1026 R²⁹ G¹⁸ 1027 R²⁹ G¹⁹ 1028 R²⁹ G²⁰ 1029 R³⁰ G¹⁷ 1030 R³⁰ G¹⁸ 1031 R³⁰ G¹⁹ 1032 R³⁰ G²⁰ 1033 R³¹ G¹⁷ 1034 R³¹ G¹⁸ 1035 R³¹ G¹⁹ 1036 R³¹ G²⁰ 1037 R³² G¹⁷ 1038 R³² G¹⁸ 1039 R³² G¹⁹ 1040 R³² G²⁰ 1041 R³³ G¹⁷ 1042 R³³ G¹⁸ 1043 R³³ G¹⁹ 1044 R³³ G²⁰ 1045 R³⁴ G¹⁷ 1046 R³⁴ G¹⁸ 1047 R³⁴ G¹⁹ 1048 R³⁴ G²⁰ 1049 R³⁵ G¹⁷ 1050 R³⁵ G¹⁸ 1051 R³⁵ G¹⁹ 1052 R³⁵ G²⁰ 1053 R³⁶ G¹⁷ 1054 R³⁶ G¹⁸ 1055 R³⁶ G¹⁹ 1056 R³⁶ G²⁰ 1057 R³⁷ G¹⁷ 1058 R³⁷ G¹⁸ 1059 R³⁷ G¹⁹ 1060 R³⁷ G²⁰ 1061 R³⁸ G¹⁷ 1062 R³⁸ G¹⁸ 1063 R³⁸ G¹⁹ 1064 R³⁸ G²⁰ 1065 R³⁹ G¹⁷ 1066 R³⁹ G¹⁸ 1067 R³⁹ G¹⁹ 1068 R³⁹ G²⁰ 1069 R⁴⁰ G¹⁷ 1070 R⁴⁰ G¹⁸ 1071 R⁴⁰ G¹⁹ 1072 R⁴⁰ G²⁰ 1073 R⁴¹ G¹⁷ 1074 R⁴¹ G¹⁸ 1075 R⁴¹ G¹⁹ 1076 R⁴¹ G²⁰ 1077 R⁴² G¹⁷ 1078 R⁴² G¹⁸ 1079 R⁴² G¹⁹ 1080 R⁴² G²⁰ 1081 R⁴³ G¹⁷ 1082 R⁴³ G¹⁸ 1083 R⁴³ G¹⁹ 1084 R⁴³ G²⁰ 1085 R⁴⁴ G¹⁷ 1086 R⁴⁴ G¹⁸ 1087 R⁴⁴ G¹⁹ 1088 R⁴⁴ G²⁰ 1089 R⁴⁵ G¹⁷ 1090 R⁴⁵ G¹⁸ 1091 R⁴⁵ G¹⁹ 1092 R⁴⁵ G²⁰ 1093 R⁴⁶ G¹⁷ 1094 R⁴⁶ G¹⁸ 1095 R⁴⁶ G¹⁹ 1096 R⁴⁶ G²⁰ 1097 R⁴⁷ G¹⁷ 1098 R⁴⁷ G¹⁸ 1099 R⁴⁷ G¹⁹ 1100 R⁴⁷ G²⁰ 1101 R⁴⁸ G¹⁷ 1102 R⁴⁸ G¹⁸ 1103 R⁴⁸ G¹⁹ 1104 R⁴⁸ G²⁰ 1105 R⁴⁹ G¹⁷ 1106 R⁴⁹ G¹⁸ 1107 R⁴⁹ G¹⁹ 1108 R⁴⁹ G²⁰ 1109 R⁵⁰ G¹⁷ 1110 R⁵⁰ G¹⁸ 1111 R⁵⁰ G¹⁹ 1112 R⁵⁰ G²⁰ 1113 R⁵¹ G¹⁷ 1114 R⁵¹ G¹⁸ 1115 R⁵¹ G¹⁹ 1116 R⁵¹ G²⁰ 1117 R⁵² G¹⁷ 1118 R⁵² G¹⁸ 1119 R⁵² G¹⁹ 1120 R⁵² G²⁰ 1121 R⁵³ G¹⁷ 1122 R⁵³ G¹⁸ 1123 R⁵³ G¹⁹ 1124 R⁵³ G²⁰ 1125 R⁵⁴ G¹⁷ 1126 R⁵⁴ G¹⁸ 1127 R⁵⁴ G¹⁹ 1128 R⁵⁴ G²⁰ 1129 R⁵⁵ G¹⁷ 1130 R⁵⁵ G¹⁸ 1131 R⁵⁵ G¹⁹ 1132 R⁵⁵ G²⁰ 1133 R⁵⁶ G¹⁷ 1134 R⁵⁶ G¹⁸ 1135 R⁵⁶ G¹⁹ 1136 R⁵⁶ G²⁰ 1137 R⁵⁷ G¹⁷ 1138 R⁵⁷ G¹⁸ 1139 R⁵⁷ G¹⁹ 1140 R⁵⁷ G²⁰ 1141 R¹ G²¹ 1142 R¹ G²² 1143 R¹ G²³ 1144 R¹ G²⁴ 1145 R² G²¹ 1146 R² G²² 1147 R² G²³ 1148 R² G²⁴ 1149 R³ G²¹ 1150 R³ G²² 1151 R³ G²³ 1152 R³ G²⁴ 1153 R⁴ G²¹ 1154 R⁴ G²² 1155 R⁴ G²³ 1156 R⁴ G²⁴ 1157 R⁵ G²¹ 1158 R⁵ G²² 1159 R⁵ G²³ 1160 R⁵ G²⁴ 1161 R⁶ G²¹ 1162 R⁶ G²² 1163 R⁶ G²³ 1164 R⁶ G²⁴ 1165 R⁷ G²¹ 1166 R⁷ G²² 1167 R⁷ G²³ 1168 R⁷ G²⁴ 1169 R⁸ G²¹ 1170 R⁸ G²² 1171 R⁸ G²³ 1172 R⁸ G²⁴ 1173 R⁹ G²¹ 1174 R⁹ G²² 1175 R⁹ G²³ 1176 R⁹ G²⁴ 1177 R¹⁰ G²¹ 1178 R¹⁰ G²² 1179 R¹⁰ G²³ 1180 R¹⁰ G²⁴ 1181 R¹¹ G²¹ 1182 R¹¹ G²² 1183 R¹¹ G²³ 1184 R¹¹ G²⁴ 1185 R¹² G²¹ 1186 R¹² G²² 1187 R¹² G²³ 1188 R¹² G²⁴ 1189 R¹³ G²¹ 1190 R¹³ G²² 1191 R¹³ G²³ 1192 R¹³ G²⁴ 1193 R¹⁴ G²¹ 1194 R¹⁴ G²² 1195 R¹⁴ G²³ 1196 R¹⁴ G²⁴ 1197 R¹⁵ G²¹ 1198 R¹⁵ G²² 1199 R¹⁵ G²³ 1200 R¹⁵ G²⁴ 1201 R¹⁶ G²¹ 1202 R¹⁶ G²² 1203 R¹⁶ G²³ 1204 R¹⁶ G²⁴ 1205 R¹⁷ G²¹ 1206 R¹⁷ G²² 1207 R¹⁷ G²³ 1208 R¹⁷ G²⁴ 1209 R¹⁸ G²¹ 1210 R¹⁸ G²² 1211 R¹⁸ G²³ 1212 R¹⁸ G²⁴ 1213 R¹⁹ G²¹ 1214 R¹⁹ G²² 1215 R¹⁹ G²³ 1216 R¹⁹ G²⁴ 1217 R²⁰ G²¹ 1218 R²⁰ G²² 1219 R²⁰ G²³ 1220 R²⁰ G²⁴ 1221 R²¹ G²¹ 1222 R²¹ G²² 1223 R²¹ G²³ 1224 R²¹ G²⁴ 1225 R²² G²¹ 1226 R²² G²² 1227 R²² G²³ 1228 R²² G²⁴ 1229 R²³ G²¹ 1230 R²³ G²² 1231 R²³ G²³ 1232 R²³ G²⁴ 1233 R²⁴ G²¹ 1234 R²⁴ G²² 1235 R²⁴ G²³ 1236 R²⁴ G²⁴ 1237 R²⁵ G²¹ 1238 R²⁵ G²² 1239 R²⁵ G²³ 1240 R²⁵ G²⁴ 1241 R²⁶ G²¹ 1242 R²⁶ G²² 1243 R²⁶ G²³ 1244 R²⁶ G²⁴ 1245 R²⁷ G²¹ 1246 R²⁷ G²² 1247 R²⁷ G²³ 1248 R²⁷ G²⁴ 1249 R²⁸ G²¹ 1250 R²⁸ G²² 1251 R²⁸ G²³ 1252 R²⁸ G²⁴ 1253 R²⁹ G²¹ 1254 R²⁹ G²² 1255 R²⁹ G²³ 1256 R²⁹ G²⁴ 1257 R³⁰ G²¹ 1258 R³⁰ G²² 1259 R³⁰ G²³ 1260 R³⁰ G²⁴ 1261 R³¹ G²¹ 1262 R³¹ G²² 1263 R³¹ G²³ 1264 R³¹ G²⁴ 1265 R³² G²¹ 1266 R³² G²² 1267 R³² G²³ 1268 R³² G²⁴ 1269 R³³ G²¹ 1270 R³³ G²² 1271 R³³ G²³ 1272 R³³ G²⁴ 1273 R³⁴ G²¹ 1274 R³⁴ G²² 1275 R³⁴ G²³ 1276 R³⁴ G²⁴ 1277 R³⁵ G²¹ 1278 R³⁵ G²² 1279 R³⁵ G²³ 1280 R³⁵ G²⁴ 1281 R³⁶ G²¹ 1282 R³⁶ G²² 1283 R³⁶ G²³ 1284 R³⁶ G²⁴ 1285 R³⁷ G²¹ 1286 R³⁷ G²² 1287 R³⁷ G²³ 1288 R³⁷ G²⁴ 1289 R³⁸ G²¹ 1290 R³⁸ G²² 1291 R³⁸ G²³ 1292 R³⁸ G²⁴ 1293 R³⁹ G²¹ 1294 R³⁹ G²² 1295 R³⁹ G²³ 1296 R³⁹ G²⁴ 1297 R⁴⁰ G²¹ 1298 R⁴⁰ G²² 1299 R⁴⁰ G²³ 1300 R⁴⁰ G²⁴ 1301 R⁴¹ G²¹ 1302 R⁴¹ G²² 1303 R⁴¹ G²³ 1304 R⁴¹ G²⁴ 1305 R⁴² G²¹ 1306 R⁴² G²² 1307 R⁴² G²³ 1308 R⁴² G²⁴ 1309 R⁴³ G²¹ 1310 R⁴³ G²² 1311 R⁴³ G²³ 1312 R⁴³ G²⁴ 1313 R⁴⁴ G²¹ 1314 R⁴⁴ G²² 1315 R⁴⁴ G²³ 1316 R⁴⁴ G²⁴ 1317 R⁴⁵ G²¹ 1318 R⁴⁵ G²² 1319 R⁴⁵ G²³ 1320 R⁴⁵ G²⁴ 1321 R⁴⁶ G²¹ 1322 R⁴⁶ G²² 1323 R⁴⁶ G²³ 1324 R⁴⁶ G²⁴ 1325 R⁴⁷ G²¹ 1326 R⁴⁷ G²² 1327 R⁴⁷ G²³ 1328 R⁴⁷ G²⁴ 1329 R⁴⁸ G²¹ 1330 R⁴⁸ G²² 1331 R⁴⁸ G²³ 1332 R⁴⁸ G²⁴ 1333 R⁴⁹ G²¹ 1334 R⁴⁹ G²² 1335 R⁴⁹ G²³ 1336 R⁴⁹ G²⁴ 1337 R⁵⁰ G²¹ 1338 R⁵⁰ G²² 1339 R⁵⁰ G²³ 1340 R⁵⁰ G²⁴ 1341 R⁵¹ G²¹ 1342 R⁵¹ G²² 1343 R⁵¹ G²³ 1344 R⁵¹ G²⁴ 1345 R⁵² G²¹ 1346 R⁵² G²² 1347 R⁵² G²³ 1348 R⁵² G²⁴ 1349 R⁵³ G²¹ 1350 R⁵³ G²² 1351 R⁵³ G²³ 1352 R⁵³ G²⁴ 1353 R⁵⁴ G²¹ 1354 R⁵⁴ G²² 1355 R⁵⁴ G²³ 1356 R⁵⁴ G²⁴ 1357 R⁵⁵ G²¹ 1358 R⁵⁵ G²² 1359 R⁵⁵ G²³ 1360 R⁵⁵ G²⁴ 1361 R⁵⁶ G²¹ 1362 R⁵⁶ G²² 1363 R⁵⁶ G²³ 1364 R⁵⁶ G²⁴ 1365 R⁵⁷ G²¹ 1366 R⁵⁷ G²² 1367 R⁵⁷ G²³ 1368 R⁵⁷ G²⁴ 1369 R¹ G²⁵ 1370 R¹ G²⁶ 1371 R¹ G²⁷ 1372 R¹ G²⁸ 1373 R² G²⁵ 1374 R² G²⁶ 1375 R² G²⁷ 1376 R² G²⁸ 1377 R³ G²⁵ 1378 R³ G²⁶ 1379 R³ G²⁷ 1380 R³ G²⁸ 1381 R⁴ G²⁵ 1382 R⁴ G²⁶ 1383 R⁴ G²⁷ 1384 R⁴ G²⁸ 1385 R⁵ G²⁵ 1386 R⁵ G²⁶ 1387 R⁵ G²⁷ 1388 R⁵ G²⁸ 1389 R⁶ G²⁵ 1390 R⁶ G²⁶ 1391 R⁶ G²⁷ 1392 R⁶ G²⁸ 1393 R⁷ G²⁵ 1394 R⁷ G²⁶ 1395 R⁷ G²⁷ 1396 R⁷ G²⁸ 1397 R⁸ G²⁵ 1398 R⁸ G²⁶ 1399 R⁸ G²⁷ 1400 R⁸ G²⁸ 1401 R⁹ G²⁵ 1402 R⁹ G²⁶ 1403 R⁹ G²⁷ 1404 R⁹ G²⁸ 1405 R¹⁰ G²⁵ 1406 R¹⁰ G²⁶ 1407 R¹⁰ G²⁷ 1408 R¹⁰ G²⁸ 1409 R¹¹ G²⁵ 1410 R¹¹ G²⁶ 1411 R¹¹ G²⁷ 1412 R¹¹ G²⁸ 1413 R¹² G²⁵ 1414 R¹² G²⁶ 1415 R¹² G²⁷ 1416 R¹² G²⁸ 1417 R¹³ G²⁵ 1418 R¹³ G²⁶ 1419 R¹³ G²⁷ 1420 R¹³ G²⁸ 1421 R¹⁴ G²⁵ 1422 R¹⁴ G²⁶ 1423 R¹⁴ G²⁷ 1424 R¹⁴ G²⁸ 1425 R¹⁵ G²⁵ 1426 R¹⁵ G²⁶ 1427 R¹⁵ G²⁷ 1428 R¹⁵ G²⁸ 1429 R¹⁶ G²⁵ 1430 R¹⁶ G²⁶ 1431 R¹⁶ G²⁷ 1432 R¹⁶ G²⁸ 1433 R¹⁷ G²⁵ 1434 R¹⁷ G²⁶ 1435 R¹⁷ G²⁷ 1436 R¹⁷ G²⁸ 1437 R¹⁸ G²⁵ 1438 R¹⁸ G²⁶ 1439 R¹⁸ G²⁷ 1440 R¹⁸ G²⁸ 1441 R¹⁹ G²⁵ 1442 R¹⁹ G²⁶ 1443 R¹⁹ G²⁷ 1444 R¹⁹ G²⁸ 1445 R²⁰ G²⁵ 1446 R²⁰ G²⁶ 1447 R²⁰ G²⁷ 1448 R²⁰ G²⁸ 1449 R²¹ G²⁵ 1450 R²¹ G²⁶ 1451 R²¹ G²⁷ 1452 R²¹ G²⁸ 1453 R²² G²⁵ 1454 R²² G²⁶ 1455 R²² G²⁷ 1456 R²² G²⁸ 1457 R²³ G²⁵ 1458 R²³ G²⁶ 1459 R²³ G²⁷ 1460 R²³ G²⁸ 1461 R²⁴ G²⁵ 1462 R²⁴ G²⁶ 1463 R²⁴ G²⁷ 1464 R²⁴ G²⁸ 1465 R²⁵ G²⁵ 1466 R²⁵ G²⁶ 1467 R²⁵ G²⁷ 1468 R²⁵ G²⁸ 1469 R²⁶ G²⁵ 1470 R²⁶ G²⁶ 1471 R²⁶ G²⁷ 1472 R²⁶ G²⁸ 1473 R²⁷ G²⁵ 1474 R²⁷ G²⁶ 1475 R²⁷ G²⁷ 1476 R²⁷ G²⁸ 1477 R²⁸ G²⁵ 1478 R²⁸ G²⁶ 1479 R²⁸ G²⁷ 1480 R²⁸ G²⁸ 1481 R²⁹ G²⁵ 1482 R²⁹ G²⁶ 1483 R²⁹ G²⁷ 1484 R²⁹ G²⁸ 1485 R³⁰ G²⁵ 1486 R³⁰ G²⁶ 1487 R³⁰ G²⁷ 1488 R³⁰ G²⁸ 1489 R³¹ G²⁵ 1490 R³¹ G²⁶ 1491 R³¹ G²⁷ 1492 R³¹ G²⁸ 1493 R³² G²⁵ 1494 R³² G²⁶ 1495 R³² G²⁷ 1496 R³² G²⁸ 1497 R³³ G²⁵ 1498 R³³ G²⁶ 1499 R³³ G²⁷ 1500 R³³ G²⁸ 1501 R³⁴ G²⁵ 1502 R³⁴ G²⁶ 1503 R³⁴ G²⁷ 1504 R³⁴ G²⁸ 1505 R³⁵ G²⁵ 1506 R³⁵ G²⁶ 1507 R³⁵ G²⁷ 1508 R³⁵ G²⁸ 1509 R³⁶ G²⁵ 1510 R³⁶ G²⁶ 1511 R³⁶ G²⁷ 1512 R³⁶ G²⁸ 1513 R³⁷ G²⁵ 1514 R³⁷ G²⁶ 1515 R³⁷ G²⁷ 1516 R³⁷ G²⁸ 1517 R³⁸ G²⁵ 1518 R³⁸ G²⁶ 1519 R³⁸ G²⁷ 1520 R³⁸ G²⁸ 1521 R³⁹ G²⁵ 1522 R³⁹ G²⁶ 1523 R³⁹ G²⁷ 1524 R³⁹ G²⁸ 1525 R⁴⁰ G²⁵ 1526 R⁴⁰ G²⁶ 1527 R⁴⁰ G²⁷ 1528 R⁴⁰ G²⁸ 1529 R⁴¹ G²⁵ 1530 R⁴¹ G²⁶ 1531 R⁴¹ G²⁷ 1532 R⁴¹ G²⁸ 1533 R⁴² G²⁵ 1534 R⁴² G²⁶ 1535 R⁴² G²⁷ 1536 R⁴² G²⁸ 1537 R⁴³ G²⁵ 1538 R⁴³ G²⁶ 1539 R⁴³ G²⁷ 1540 R⁴³ G²⁸ 1541 R⁴⁴ G²⁵ 1542 R⁴⁴ G²⁶ 1543 R⁴⁴ G²⁷ 1544 R⁴⁴ G²⁸ 1545 R⁴⁵ G²⁵ 1546 R⁴⁵ G²⁶ 1547 R⁴⁵ G²⁷ 1548 R⁴⁵ G²⁸ 1549 R⁴⁶ G²⁵ 1550 R⁴⁶ G²⁶ 1551 R⁴⁶ G²⁷ 1552 R⁴⁶ G²⁸ 1553 R⁴⁷ G²⁵ 1554 R⁴⁷ G²⁶ 1555 R⁴⁷ G²⁷ 1556 R⁴⁷ G²⁸ 1557 R⁴⁸ G²⁵ 1558 R⁴⁸ G²⁶ 1559 R⁴⁸ G²⁷ 1560 R⁴⁸ G²⁸ 1561 R⁴⁹ G²⁵ 1562 R⁴⁹ G²⁶ 1563 R⁴⁹ G²⁷ 1564 R⁴⁹ G²⁸ 1565 R⁵⁰ G²⁵ 1566 R⁵⁰ G²⁶ 1567 R⁵⁰ G²⁷ 1568 R⁵⁰ G²⁸ 1569 R⁵¹ G²⁵ 1570 R⁵¹ G²⁶ 1571 R⁵¹ G²⁷ 1572 R⁵¹ G²⁸ 1573 R⁵² G²⁵ 1574 R⁵² G²⁶ 1575 R⁵² G²⁷ 1576 R⁵² G²⁸ 1577 R⁵³ G²⁵ 1578 R⁵³ G²⁶ 1579 R⁵³ G²⁷ 1580 R⁵³ G²⁸ 1581 R⁵⁴ G²⁵ 1582 R⁵⁴ G²⁶ 1583 R⁵⁴ G²⁷ 1584 R⁵⁴ G²⁸ 1585 R⁵⁵ G²⁵ 1586 R⁵⁵ G²⁶ 1587 R⁵⁵ G²⁷ 1588 R⁵⁵ G²⁸ 1589 R⁵⁶ G²⁵ 1590 R⁵⁶ G²⁶ 1591 R⁵⁶ G²⁷ 1592 R⁵⁶ G²⁸ 1593 R⁵⁷ G²⁵ 1594 R⁵⁷ G²⁶ 1595 R⁵⁷ G²⁷ 1596 R⁵⁷ G²⁸ 1597 R¹ G²⁹ 1598 R¹ G³⁰ 1599 R¹ G³¹ 1600 R¹ G³² 1601 R² G²⁹ 1602 R² G³⁰ 1603 R² G³¹ 1604 R² G³² 1605 R³ G²⁹ 1606 R³ G³⁰ 1607 R³ G³¹ 1608 R³ G³² 1609 R⁴ G²⁹ 1610 R⁴ G³⁰ 1611 R⁴ G³¹ 1612 R⁴ G³² 1613 R⁵ G²⁹ 1614 R⁵ G³⁰ 1615 R⁵ G³¹ 1616 R⁵ G³² 1617 R⁶ G²⁹ 1618 R⁶ G³⁰ 1619 R⁶ G³¹ 1620 R⁶ G³² 1621 R⁷ G²⁹ 1622 R⁷ G³⁰ 1623 R⁷ G³¹ 1624 R⁷ G³² 1625 R⁸ G²⁹ 1626 R⁸ G³⁰ 1627 R⁸ G³¹ 1628 R⁸ G³² 1629 R⁹ G²⁹ 1630 R⁹ G³⁰ 1631 R⁹ G³¹ 1632 R⁹ G³² 1633 R¹⁰ G²⁹ 1634 R¹⁰ G³⁰ 1635 R¹⁰ G³¹ 1636 R¹⁰ G³² 1637 R¹¹ G²⁹ 1638 R¹¹ G³⁰ 1639 R¹¹ G³¹ 1640 R¹¹ G³² 1641 R¹² G²⁹ 1642 R¹² G³⁰ 1643 R¹² G³¹ 1644 R¹² G³² 1645 R¹³ G²⁹ 1646 R¹³ G³⁰ 1647 R¹³ G³¹ 1648 R¹³ G³² 1649 R¹⁴ G²⁹ 1650 R¹⁴ G³⁰ 1651 R¹⁴ G³¹ 1652 R¹⁴ G³² 1653 R¹⁵ G²⁹ 1654 R¹⁵ G³⁰ 1655 R¹⁵ G³¹ 1656 R¹⁵ G³² 1657 R¹⁶ G²⁹ 1658 R¹⁶ G³⁰ 1659 R¹⁶ G³¹ 1660 R¹⁶ G³² 1661 R¹⁷ G²⁹ 1662 R¹⁷ G³⁰ 1663 R¹⁷ G³¹ 1664 R¹⁷ G³² 1665 R¹⁸ G²⁹ 1666 R¹⁸ G³⁰ 1667 R¹⁸ G³¹ 1668 R¹⁸ G³² 1669 R¹⁹ G²⁹ 1670 R¹⁹ G³⁰ 1671 R¹⁹ G³¹ 1672 R¹⁹ G³² 1673 R²⁰ G²⁹ 1674 R²⁰ G³⁰ 1675 R²⁰ G³¹ 1676 R²⁰ G³² 1677 R²¹ G²⁹ 1678 R²¹ G³⁰ 1679 R²¹ G³¹ 1680 R²¹ G³² 1681 R²² G²⁹ 1682 R²² G³⁰ 1683 R²² G³¹ 1684 R²² G³² 1685 R²³ G²⁹ 1686 R²³ G³⁰ 1687 R²³ G³¹ 1688 R²³ G³² 1689 R²⁴ G²⁹ 1690 R²⁴ G³⁰ 1691 R²⁴ G³¹ 1692 R²⁴ G³² 1693 R²⁵ G²⁹ 1694 R²⁵ G³⁰ 1695 R²⁵ G³¹ 1696 R²⁵ G³² 1697 R²⁶ G²⁹ 1698 R²⁶ G³⁰ 1699 R²⁶ G³¹ 1700 R²⁶ G³² 1701 R²⁷ G²⁹ 1702 R²⁷ G³⁰ 1703 R²⁷ G³¹ 1704 R²⁷ G³² 1705 R²⁸ G²⁹ 1706 R²⁸ G³⁰ 1707 R²⁸ G³¹ 1708 R²⁸ G³² 1709 R²⁹ G²⁹ 1710 R²⁹ G³⁰ 1711 R²⁹ G³¹ 1712 R²⁹ G³² 1713 R³⁰ G²⁹ 1714 R³⁰ G³⁰ 1715 R³⁰ G³¹ 1716 R³⁰ G³² 1717 R³¹ G²⁹ 1718 R³¹ G³⁰ 1719 R³¹ G³¹ 1720 R³¹ G³² 1721 R³² G²⁹ 1722 R³² G³⁰ 1723 R³² G³¹ 1724 R³² G³² 1725 R³³ G²⁹ 1726 R³³ G³⁰ 1727 R³³ G³¹ 1728 R³³ G³² 1729 R³⁴ G²⁹ 1730 R³⁴ G³⁰ 1731 R³⁴ G³¹ 1732 R³⁴ G³² 1733 R³⁵ G²⁹ 1734 R³⁵ G³⁰ 1735 R³⁵ G³¹ 1736 R³⁵ G³² 1737 R³⁶ G²⁹ 1738 R³⁶ G³⁰ 1739 R³⁶ G³¹ 1740 R³⁶ G³² 1741 R³⁷ G²⁹ 1742 R³⁷ G³⁰ 1743 R³⁷ G³¹ 1744 R³⁷ G³² 1745 R³⁸ G²⁹ 1746 R³⁸ G³⁰ 1747 R³⁸ G³¹ 1748 R³⁸ G³² 1749 R³⁹ G²⁹ 1750 R³⁹ G³⁰ 1751 R³⁹ G³¹ 1752 R³⁹ G³² 1753 R⁴⁰ G²⁹ 1754 R⁴⁰ G³⁰ 1755 R⁴⁰ G³¹ 1756 R⁴⁰ G³² 1757 R⁴¹ G²⁹ 1758 R⁴¹ G³⁰ 1759 R⁴¹ G³¹ 1760 R⁴¹ G³² 1761 R⁴² G²⁹ 1762 R⁴² G³⁰ 1763 R⁴² G³¹ 1764 R⁴² G³² 1765 R⁴³ G²⁹ 1766 R⁴³ G³⁰ 1767 R⁴³ G³¹ 1768 R⁴³ G³² 1769 R⁴⁴ G²⁹ 1770 R⁴⁴ G³⁰ 1771 R⁴⁴ G³¹ 1772 R⁴⁴ G³² 1773 R⁴⁵ G²⁹ 1774 R⁴⁵ G³⁰ 1775 R⁴⁵ G³¹ 1776 R⁴⁵ G³² 1777 R⁴⁶ G²⁹ 1778 R⁴⁶ G³⁰ 1779 R⁴⁶ G³¹ 1780 R⁴⁶ G³² 1781 R⁴⁷ G²⁹ 1782 R⁴⁷ G³⁰ 1783 R⁴⁷ G³¹ 1784 R⁴⁷ G³² 1785 R⁴⁸ G²⁹ 1786 R⁴⁸ G³⁰ 1787 R⁴⁸ G³¹ 1788 R⁴⁸ G³² 1789 R⁴⁹ G²⁹ 1790 R⁴⁹ G³⁰ 1791 R⁴⁹ G³¹ 1792 R⁴⁹ G³² 1793 R⁵⁰ G²⁹ 1794 R⁵⁰ G³⁰ 1795 R⁵⁰ G³¹ 1796 R⁵⁰ G³² 1797 R⁵¹ G²⁹ 1798 R⁵¹ G³⁰ 1799 R⁵¹ G³¹ 1800 R⁵¹ G³² 1801 R⁵² G²⁹ 1802 R⁵² G³⁰ 1803 R⁵² G³¹ 1804 R⁵² G³² 1805 R⁵³ G²⁹ 1806 R⁵³ G³⁰ 1807 R⁵³ G³¹ 1808 R⁵³ G³² 1809 R⁵⁴ G²⁹ 1810 R⁵⁴ G³⁰ 1811 R⁵⁴ G³¹ 1812 R⁵⁴ G³² 1813 R⁵⁵ G²⁹ 1814 R⁵⁵ G³⁰ 1815 R⁵⁵ G³¹ 1816 R⁵⁵ G³² 1817 R⁵⁶ G²⁹ 1818 R⁵⁶ G³⁰ 1819 R⁵⁶ G³¹ 1820 R⁵⁶ G³² 1821 R⁵⁷ G²⁹ 1822 R⁵⁷ G³⁰ 1823 R⁵⁷ G³¹ 1824 R⁵⁷ G³² 1825 R¹ G³³ 1826 R¹ G³⁴ 1827 R¹ G³⁵ 1828 R¹ G³⁶ 1829 R² G³³ 1830 R² G³⁴ 1831 R² G³⁵ 1832 R² G³⁶ 1833 R³ G³³ 1834 R³ G³⁴ 1835 R³ G³⁵ 1836 R³ G³⁶ 1837 R⁴ G³³ 1838 R⁴ G³⁴ 1839 R⁴ G³⁵ 1840 R⁴ G³⁶ 1841 R⁵ G³³ 1842 R⁵ G³⁴ 1843 R⁵ G³⁵ 1844 R⁵ G³⁶ 1845 R⁶ G³³ 1846 R⁶ G³⁴ 1847 R⁶ G³⁵ 1848 R⁶ G³⁶ 1849 R⁷ G³³ 1850 R⁷ G³⁴ 1851 R⁷ G³⁵ 1852 R⁷ G³⁶ 1853 R⁸ G³³ 1854 R⁸ G³⁴ 1855 R⁸ G³⁵ 1856 R⁸ G³⁶ 1857 R⁹ G³³ 1858 R⁹ G³⁴ 1859 R⁹ G³⁵ 1860 R⁹ G³⁶ 1861 R¹⁰ G³³ 1862 R¹⁰ G³⁴ 1863 R¹⁰ G³⁵ 1864 R¹⁰ G³⁶ 1865 R¹¹ G³³ 1866 R¹¹ G³⁴ 1867 R¹¹ G³⁵ 1868 R¹¹ G³⁶ 1869 R¹² G³³ 1870 R¹² G³⁴ 1871 R¹² G³⁵ 1872 R¹² G³⁶ 1873 R¹³ G³³ 1874 R¹³ G³⁴ 1875 R¹³ G³⁵ 1876 R¹³ G³⁶ 1877 R¹⁴ G³³ 1878 R¹⁴ G³⁴ 1879 R¹⁴ G³⁵ 1880 R¹⁴ G³⁶ 1881 R¹⁵ G³³ 1882 R¹⁵ G³⁴ 1883 R¹⁵ G³⁵ 1884 R¹⁵ G³⁶ 1885 R¹⁶ G³³ 1886 R¹⁶ G³⁴ 1887 R¹⁶ G³⁵ 1888 R¹⁶ G³⁶ 1889 R¹⁷ G³³ 1890 R¹⁷ G³⁴ 1891 R¹⁷ G³⁵ 1892 R¹⁷ G³⁶ 1893 R¹⁸ G³³ 1894 R¹⁸ G³⁴ 1895 R¹⁸ G³⁵ 1896 R¹⁸ G³⁶ 1897 R¹⁹ G³³ 1898 R¹⁹ G³⁴ 1899 R¹⁹ G³⁵ 1900 R¹⁹ G³⁶ 1901 R²⁰ G³³ 1902 R²⁰ G³⁴ 1903 R²⁰ G³⁵ 1904 R²⁰ G³⁶ 1905 R²¹ G³³ 1906 R²¹ G³⁴ 1907 R²¹ G³⁵ 1908 R²¹ G³⁶ 1909 R²² G³³ 1910 R²² G³⁴ 1911 R²² G³⁵ 1912 R²² G³⁶ 1913 R²³ G³³ 1914 R²³ G³⁴ 1915 R²³ G³⁵ 1916 R²³ G³⁶ 1917 R²⁴ G³³ 1918 R²⁴ G³⁴ 1919 R²⁴ G³⁵ 1920 R²⁴ G³⁶ 1921 R²⁵ G³³ 1922 R²⁵ G³⁴ 1923 R²⁵ G³⁵ 1924 R²⁵ G³⁶ 1925 R²⁶ G³³ 1926 R²⁶ G³⁴ 1927 R²⁶ G³⁵ 1928 R²⁶ G³⁶ 1929 R²⁷ G³³ 1930 R²⁷ G³⁴ 1931 R²⁷ G³⁵ 1932 R²⁷ G³⁶ 1933 R²⁸ G³³ 1934 R²⁸ G³⁴ 1935 R²⁸ G³⁵ 1936 R²⁸ G³⁶ 1937 R²⁹ G³³ 1938 R²⁹ G³⁴ 1939 R²⁹ G³⁵ 1940 R²⁹ G³⁶ 1941 R³⁰ G³³ 1942 R³⁰ G³⁴ 1943 R³⁰ G³⁵ 1944 R³⁰ G³⁶ 1945 R³¹ G³³ 1946 R³¹ G³⁴ 1947 R³¹ G³⁵ 1948 R³¹ G³⁶ 1949 R³² G³³ 1950 R³² G³⁴ 1951 R³² G³⁵ 1952 R³² G³⁶ 1953 R³³ G³³ 1954 R³³ G³⁴ 1955 R³³ G³⁵ 1956 R³³ G³⁶ 1957 R³⁴ G³³ 1958 R³⁴ G³⁴ 1959 R³⁴ G³⁵ 1960 R³⁴ G³⁶ 1961 R³⁵ G³³ 1962 R³⁵ G³⁴ 1963 R³⁵ G³⁵ 1964 R³⁵ G³⁶ 1965 R³⁶ G³³ 1966 R³⁶ G³⁴ 1967 R³⁶ G³⁵ 1968 R³⁶ G³⁶ 1969 R³⁷ G³³ 1970 R³⁷ G³⁴ 1971 R³⁷ G³⁵ 1972 R³⁷ G³⁶ 1973 R³⁸ G³³ 1974 R³⁸ G³⁴ 1975 R³⁸ G³⁵ 1976 R³⁸ G³⁶ 1977 R³⁹ G³³ 1978 R³⁹ G³⁴ 1979 R³⁹ G³⁵ 1980 R³⁹ G³⁶ 1981 R⁴⁰ G³³ 1982 R⁴⁰ G³⁴ 1983 R⁴⁰ G³⁵ 1984 R⁴⁰ G³⁶ 1985 R⁴¹ G³³ 1986 R⁴¹ G³⁴ 1987 R⁴¹ G³⁵ 1988 R⁴¹ G³⁶ 1989 R⁴² G³³ 1990 R⁴² G³⁴ 1991 R⁴² G³⁵ 1992 R⁴² G³⁶ 1993 R⁴³ G³³ 1994 R⁴³ G³⁴ 1995 R⁴³ G³⁵ 1996 R⁴³ G³⁶ 1997 R⁴⁴ G³³ 1998 R⁴⁴ G³⁴ 1999 R⁴⁴ G³⁵ 2000 R⁴⁴ G³⁶ 2001 R⁴⁵ G³³ 2002 R⁴⁵ G³⁴ 2003 R⁴⁵ G³⁵ 2004 R⁴⁵ G³⁶ 2005 R⁴⁶ G³³ 2006 R⁴⁶ G³⁴ 2007 R⁴⁶ G³⁵ 2008 R⁴⁶ G³⁶ 2009 R⁴⁷ G³³ 2010 R⁴⁷ G³⁴ 2011 R⁴⁷ G³⁵ 2012 R⁴⁷ G³⁶ 2013 R⁴⁸ G³³ 2014 R⁴⁸ G³⁴ 2015 R⁴⁸ G³⁵ 2016 R⁴⁸ G³⁶ 2017 R⁴⁹ G³³ 2018 R⁴⁹ G³⁴ 2019 R⁴⁹ G³⁵ 2020 R⁴⁹ G³⁶ 2021 R⁵⁰ G³³ 2022 R⁵⁰ G³⁴ 2023 R⁵⁰ G³⁵ 2024 R⁵⁰ G³⁶ 2025 R⁵¹ G³³ 2026 R⁵¹ G³⁴ 2027 R⁵¹ G³⁵ 2028 R⁵¹ G³⁶ 2029 R⁵² G³³ 2030 R⁵² G³⁴ 2031 R⁵² G³⁵ 2032 R⁵² G³⁶ 2033 R⁵³ G³³ 2034 R⁵³ G³⁴ 2035 R⁵³ G³⁵ 2036 R⁵³ G³⁶ 2037 R⁵⁴ G³³ 2038 R⁵⁴ G³⁴ 2039 R⁵⁴ G³⁵ 2040 R⁵⁴ G³⁶ 2041 R⁵⁵ G³³ 2042 R⁵⁵ G³⁴ 2043 R⁵⁵ G³⁵ 2044 R⁵⁵ G³⁶ 2045 R⁵⁶ G³³ 2046 R⁵⁶ G³⁴ 2047 R⁵⁶ G³⁵ 2048 R⁵⁶ G³⁶ 2049 R⁵⁷ G³³ 2050 R⁵⁷ G³⁴ 2051 R⁵⁷ G³⁵ 2052 R⁵⁷ G³⁶ 2053 R¹ G³⁷ 2054 R¹ G³⁸ 2055 R¹ G³⁹ 2056 R¹ G⁴⁰ 2057 R² G³⁷ 2058 R² G³⁸ 2059 R² G³⁹ 2060 R² G⁴⁰ 2061 R³ G³⁷ 2062 R³ G³⁸ 2063 R³ G³⁹ 2064 R³ G⁴⁰ 2065 R⁴ G³⁷ 2066 R⁴ G³⁸ 2067 R⁴ G³⁹ 2068 R⁴ G⁴⁰ 2069 R⁵ G³⁷ 2070 R⁵ G³⁸ 2071 R⁵ G³⁹ 2072 R⁵ G⁴⁰ 2073 R⁶ G³⁷ 2074 R⁶ G³⁸ 2075 R⁶ G³⁹ 2076 R⁶ G⁴⁰ 2077 R⁷ G³⁷ 2078 R⁷ G³⁸ 2079 R⁷ G³⁹ 2080 R⁷ G⁴⁰ 2081 R⁸ G³⁷ 2082 R⁸ G³⁸ 2083 R⁸ G³⁹ 2084 R⁸ G⁴⁰ 2085 R⁹ G³⁷ 2086 R⁹ G³⁸ 2087 R⁹ G³⁹ 2088 R⁹ G⁴⁰ 2089 R¹⁰ G³⁷ 2090 R¹⁰ G³⁸ 2091 R¹⁰ G³⁹ 2092 R¹⁰ G⁴⁰ 2093 R¹¹ G³⁷ 2094 R¹¹ G³⁸ 2095 R¹¹ G³⁹ 2096 R¹¹ G⁴⁰ 2097 R¹² G³⁷ 2098 R¹² G³⁸ 2099 R¹² G³⁹ 2100 R¹² G⁴⁰ 2101 R¹³ G³⁷ 2102 R¹³ G³⁸ 2103 R¹³ G³⁹ 2104 R¹³ G⁴⁰ 2105 R¹⁴ G³⁷ 2106 R¹⁴ G³⁸ 2107 R¹⁴ G³⁹ 2108 R¹⁴ G⁴⁰ 2109 R¹⁵ G³⁷ 2110 R¹⁵ G³⁸ 2111 R¹⁵ G³⁹ 2112 R¹⁵ G⁴⁰ 2113 R¹⁶ G³⁷ 2114 R¹⁶ G³⁸ 2115 R¹⁶ G³⁹ 2116 R¹⁶ G⁴⁰ 2117 R¹⁷ G³⁷ 2118 R¹⁷ G³⁸ 2119 R¹⁷ G³⁹ 2120 R¹⁷ G⁴⁰ 2121 R¹⁸ G³⁷ 2122 R¹⁸ G³⁸ 2123 R¹⁸ G³⁹ 2124 R¹⁸ G⁴⁰ 2125 R¹⁹ G³⁷ 2126 R¹⁹ G³⁸ 2127 R¹⁹ G³⁹ 2128 R¹⁹ G⁴⁰ 2129 R²⁰ G³⁷ 2130 R²⁰ G³⁸ 2131 R²⁰ G³⁹ 2132 R²⁰ G⁴⁰ 2133 R²¹ G³⁷ 2134 R²¹ G³⁸ 2135 R²¹ G³⁹ 2136 R²¹ G⁴⁰ 2137 R²² G³⁷ 2138 R²² G³⁸ 2139 R²² G³⁹ 2140 R²² G⁴⁰ 2141 R²³ G³⁷ 2142 R²³ G³⁸ 2143 R²³ G³⁹ 2144 R²³ G⁴⁰ 2145 R²⁴ G³⁷ 2146 R²⁴ G³⁸ 2147 R²⁴ G³⁹ 2148 R²⁴ G⁴⁰ 2149 R²⁵ G³⁷ 2150 R²⁵ G³⁸ 2151 R²⁵ G³⁹ 2152 R²⁵ G⁴⁰ 2153 R²⁶ G³⁷ 2154 R²⁶ G³⁸ 2155 R²⁶ G³⁹ 2156 R²⁶ G⁴⁰ 2157 R²⁷ G³⁷ 2158 R²⁷ G³⁸ 2159 R²⁷ G³⁹ 2160 R²⁷ G⁴⁰ 2161 R²⁸ G³⁷ 2162 R²⁸ G³⁸ 2163 R²⁸ G³⁹ 2164 R²⁸ G⁴⁰ 2165 R²⁹ G³⁷ 2166 R²⁹ G³⁸ 2167 R²⁹ G³⁹ 2168 R²⁹ G⁴⁰ 2169 R³⁰ G³⁷ 2170 R³⁰ G³⁸ 2171 R³⁰ G³⁹ 2172 R³⁰ G⁴⁰ 2173 R³¹ G³⁷ 2174 R³¹ G³⁸ 2175 R³¹ G³⁹ 2176 R³¹ G⁴⁰ 2177 R³² G³⁷ 2178 R³² G³⁸ 2179 R³² G³⁹ 2180 R³² G⁴⁰ 2181 R³³ G³⁷ 2182 R³³ G³⁸ 2183 R³³ G³⁹ 2184 R³³ G⁴⁰ 2185 R³⁴ G³⁷ 2186 R³⁴ G³⁸ 2187 R³⁴ G³⁹ 2188 R³⁴ G⁴⁰ 2189 R³⁵ G³⁷ 2190 R³⁵ G³⁸ 2191 R³⁵ G³⁹ 2192 R³⁵ G⁴⁰ 2193 R³⁶ G³⁷ 2194 R³⁶ G³⁸ 2195 R³⁶ G³⁹ 2196 R³⁶ G⁴⁰ 2197 R³⁷ G³⁷ 2198 R³⁷ G³⁸ 2199 R³⁷ G³⁹ 2200 R³⁷ G⁴⁰ 2201 R³⁸ G³⁷ 2202 R³⁸ G³⁸ 2203 R³⁸ G³⁹ 2204 R³⁸ G⁴⁰ 2205 R³⁹ G³⁷ 2206 R³⁹ G³⁸ 2207 R³⁹ G³⁹ 2208 R³⁹ G⁴⁰ 2209 R⁴⁰ G³⁷ 2210 R⁴⁰ G³⁸ 2211 R⁴⁰ G³⁹ 2212 R⁴⁰ G⁴⁰ 2213 R⁴¹ G³⁷ 2214 R⁴¹ G³⁸ 2215 R⁴¹ G³⁹ 2216 R⁴¹ G⁴⁰ 2217 R⁴² G³⁷ 2218 R⁴² G³⁸ 2219 R⁴² G³⁹ 2220 R⁴² G⁴⁰ 2221 R⁴³ G³⁷ 2222 R⁴³ G³⁸ 2223 R⁴³ G³⁹ 2224 R⁴³ G⁴⁰ 2225 R⁴⁴ G³⁷ 2226 R⁴⁴ G³⁸ 2227 R⁴⁴ G³⁹ 2228 R⁴⁴ G⁴⁰ 2229 R⁴⁵ G³⁷ 2230 R⁴⁵ G³⁸ 2231 R⁴⁵ G³⁹ 2232 R⁴⁵ G⁴⁰ 2233 R⁴⁶ G³⁷ 2234 R⁴⁶ G³⁸ 2235 R⁴⁶ G³⁹ 2236 R⁴⁶ G⁴⁰ 2237 R⁴⁷ G³⁷ 2238 R⁴⁷ G³⁸ 2239 R⁴⁷ G³⁹ 2240 R⁴⁷ G⁴⁰ 2241 R⁴⁸ G³⁷ 2242 R⁴⁸ G³⁸ 2243 R⁴⁸ G³⁹ 2244 R⁴⁸ G⁴⁰ 2245 R⁴⁹ G³⁷ 2246 R⁴⁹ G³⁸ 2247 R⁴⁹ G³⁹ 2248 R⁴⁹ G⁴⁰ 2249 R⁵⁰ G³⁷ 2250 R⁵⁰ G³⁸ 2251 R⁵⁰ G³⁹ 2252 R⁵⁰ G⁴⁰ 2253 R⁵¹ G³⁷ 2254 R⁵¹ G³⁸ 2255 R⁵¹ G³⁹ 2256 R⁵¹ G⁴⁰ 2257 R⁵² G³⁷ 2258 R⁵² G³⁸ 2259 R⁵² G³⁹ 2260 R⁵² G⁴⁰ 2261 R⁵³ G³⁷ 2262 R⁵³ G³⁸ 2263 R⁵³ G³⁹ 2264 R⁵³ G⁴⁰ 2265 R⁵⁴ G³⁷ 2266 R⁵⁴ G³⁸ 2267 R⁵⁴ G³⁹ 2268 R⁵⁴ G⁴⁰ 2269 R⁵⁵ G³⁷ 2270 R⁵⁵ G³⁸ 2271 R⁵⁵ G³⁹ 2272 R⁵⁵ G⁴⁰ 2273 R⁵⁶ G³⁷ 2274 R⁵⁶ G³⁸ 2275 R⁵⁶ G³⁹ 2276 R⁵⁶ G⁴⁰ 2277 R⁵⁷ G³⁷ 2278 R⁵⁷ G³⁸ 2279 R⁵⁷ G³⁹ 2280 R⁵⁷ G⁴⁰ 2281 R¹ G⁴¹ 2282 R¹ G⁴² 2283 R¹ G⁴³ 2284 R¹ G⁴⁴ 2285 R² G⁴¹ 2286 R² G⁴² 2287 R² G⁴³ 2288 R² G⁴⁴ 2289 R³ G⁴¹ 2290 R³ G⁴² 2291 R³ G⁴³ 2292 R³ G⁴⁴ 2293 R⁴ G⁴¹ 2294 R⁴ G⁴² 2295 R⁴ G⁴³ 2296 R⁴ G⁴⁴ 2297 R⁵ G⁴¹ 2298 R⁵ G⁴² 2299 R⁵ G⁴³ 2300 R⁵ G⁴⁴ 2301 R⁶ G⁴¹ 2302 R⁶ G⁴² 2303 R⁶ G⁴³ 2304 R⁶ G⁴⁴ 2305 R⁷ G⁴¹ 2306 R⁷ G⁴² 2307 R⁷ G⁴³ 2308 R⁷ G⁴⁴ 2309 R⁸ G⁴¹ 2310 R⁸ G⁴² 2311 R⁸ G⁴³ 2312 R⁸ G⁴⁴ 2313 R⁹ G⁴¹ 2314 R⁹ G⁴² 2315 R⁹ G⁴³ 2316 R⁹ G⁴⁴ 2317 R¹⁰ G⁴¹ 2318 R¹⁰ G⁴² 2319 R¹⁰ G⁴³ 2320 R¹⁰ G⁴⁴ 2321 R¹¹ G⁴¹ 2322 R¹¹ G⁴² 2323 R¹¹ G⁴³ 2324 R¹¹ G⁴⁴ 2325 R¹² G⁴¹ 2326 R¹² G⁴² 2327 R¹² G⁴³ 2328 R¹² G⁴⁴ 2329 R¹³ G⁴¹ 2330 R¹³ G⁴² 2331 R¹³ G⁴³ 2332 R¹³ G⁴⁴ 2333 R¹⁴ G⁴¹ 2334 R¹⁴ G⁴² 2335 R¹⁴ G⁴³ 2336 R¹⁴ G⁴⁴ 2337 R¹⁵ G⁴¹ 2338 R¹⁵ G⁴² 2339 R¹⁵ G⁴³ 2340 R¹⁵ G⁴⁴ 2341 R¹⁶ G⁴¹ 2342 R¹⁶ G⁴² 2343 R¹⁶ G⁴³ 2344 R¹⁶ G⁴⁴ 2345 R¹⁷ G⁴¹ 2346 R¹⁷ G⁴² 2347 R¹⁷ G⁴³ 2348 R¹⁷ G⁴⁴ 2349 R¹⁸ G⁴¹ 2350 R¹⁸ G⁴² 2351 R¹⁸ G⁴³ 2352 R¹⁸ G⁴⁴ 2353 R¹⁹ G⁴¹ 2354 R¹⁹ G⁴² 2355 R¹⁹ G⁴³ 2356 R¹⁹ G⁴⁴ 2357 R²⁰ G⁴¹ 2358 R²⁰ G⁴² 2359 R²⁰ G⁴³ 2360 R²⁰ G⁴⁴ 2361 R²¹ G⁴¹ 2362 R²¹ G⁴² 2363 R²¹ G⁴³ 2364 R²¹ G⁴⁴ 2365 R²² G⁴¹ 2366 R²² G⁴² 2367 R²² G⁴³ 2368 R²² G⁴⁴ 2369 R²³ G⁴¹ 2370 R²³ G⁴² 2371 R²³ G⁴³ 2372 R²³ G⁴⁴ 2373 R²⁴ G⁴¹ 2374 R²⁴ G⁴² 2375 R²⁴ G⁴³ 2376 R²⁴ G⁴⁴ 2377 R²⁵ G⁴¹ 2378 R²⁵ G⁴² 2379 R²⁵ G⁴³ 2380 R²⁵ G⁴⁴ 2381 R²⁶ G⁴¹ 2382 R²⁶ G⁴² 2383 R²⁶ G⁴³ 2384 R²⁶ G⁴⁴ 2385 R²⁷ G⁴¹ 2386 R²⁷ G⁴² 2387 R²⁷ G⁴³ 2388 R²⁷ G⁴⁴ 2389 R²⁸ G⁴¹ 2390 R²⁸ G⁴² 2391 R²⁸ G⁴³ 2392 R²⁸ G⁴⁴ 2393 R²⁹ G⁴¹ 2394 R²⁹ G⁴² 2395 R²⁹ G⁴³ 2396 R²⁹ G⁴⁴ 2397 R³⁰ G⁴¹ 2398 R³⁰ G⁴² 2399 R³⁰ G⁴³ 2400 R³⁰ G⁴⁴ 2401 R³¹ G⁴¹ 2402 R³¹ G⁴² 2403 R³¹ G⁴³ 2404 R³¹ G⁴⁴ 2405 R³² G⁴¹ 2406 R³² G⁴² 2407 R³² G⁴³ 2408 R³² G⁴⁴ 2409 R³³ G⁴¹ 2410 R³³ G⁴² 2411 R³³ G⁴³ 2412 R³³ G⁴⁴ 2413 R³⁴ G⁴¹ 2414 R³⁴ G⁴² 2415 R³⁴ G⁴³ 2416 R³⁴ G⁴⁴ 2417 R³⁵ G⁴¹ 2418 R³⁵ G⁴² 2419 R³⁵ G⁴³ 2420 R³⁵ G⁴⁴ 2421 R³⁶ G⁴¹ 2422 R³⁶ G⁴² 2423 R³⁶ G⁴³ 2424 R³⁶ G⁴⁴ 2425 R³⁷ G⁴¹ 2426 R³⁷ G⁴² 2427 R³⁷ G⁴³ 2428 R³⁷ G⁴⁴ 2429 R³⁸ G⁴¹ 2430 R³⁸ G⁴² 2431 R³⁸ G⁴³ 2432 R³⁸ G⁴⁴ 2433 R³⁹ G⁴¹ 2434 R³⁹ G⁴² 2435 R³⁹ G⁴³ 2436 R³⁹ G⁴⁴ 2437 R⁴⁰ G⁴¹ 2438 R⁴⁰ G⁴² 2439 R⁴⁰ G⁴³ 2440 R⁴⁰ G⁴⁴ 2441 R⁴¹ G⁴¹ 2442 R⁴¹ G⁴² 2443 R⁴¹ G⁴³ 2444 R⁴¹ G⁴⁴ 2445 R⁴² G⁴¹ 2446 R⁴² G⁴² 2447 R⁴² G⁴³ 2448 R⁴² G⁴⁴ 2449 R⁴³ G⁴¹ 2450 R⁴³ G⁴² 2451 R⁴³ G⁴³ 2452 R⁴³ G⁴⁴ 2453 R⁴⁴ G⁴¹ 2454 R⁴⁴ G⁴² 2455 R⁴⁴ G⁴³ 2456 R⁴⁴ G⁴⁴ 2457 R⁴⁵ G⁴¹ 2458 R⁴⁵ G⁴² 2459 R⁴⁵ G⁴³ 2460 R⁴⁵ G⁴⁴ 2461 R⁴⁶ G⁴¹ 2462 R⁴⁶ G⁴² 2463 R⁴⁶ G⁴³ 2464 R⁴⁶ G⁴⁴ 2465 R⁴⁷ G⁴¹ 2466 R⁴⁷ G⁴² 2467 R⁴⁷ G⁴³ 2468 R⁴⁷ G⁴⁴ 2469 R⁴⁸ G⁴¹ 2470 R⁴⁸ G⁴² 2471 R⁴⁸ G⁴³ 2472 R⁴⁸ G⁴⁴ 2473 R⁴⁹ G⁴¹ 2474 R⁴⁹ G⁴² 2475 R⁴⁹ G⁴³ 2476 R⁴⁹ G⁴⁴ 2477 R⁵⁰ G⁴¹ 2478 R⁵⁰ G⁴² 2479 R⁵⁰ G⁴³ 2480 R⁵⁰ G⁴⁴ 2481 R⁵¹ G⁴¹ 2482 R⁵¹ G⁴² 2483 R⁵¹ G⁴³ 2484 R⁵¹ G⁴⁴ 2485 R⁵² G⁴¹ 2486 R⁵² G⁴² 2487 R⁵² G⁴³ 2488 R⁵² G⁴⁴ 2489 R⁵³ G⁴¹ 2490 R⁵³ G⁴² 2491 R⁵³ G⁴³ 2492 R⁵³ G⁴⁴ 2493 R⁵⁴ G⁴¹ 2494 R⁵⁴ G⁴² 2495 R⁵⁴ G⁴³ 2496 R⁵⁴ G⁴⁴ 2497 R⁵⁵ G⁴¹ 2498 R⁵⁵ G⁴² 2499 R⁵⁵ G⁴³ 2500 R⁵⁵ G⁴⁴ 2501 R⁵⁶ G⁴¹ 2502 R⁵⁶ G⁴² 2503 R⁵⁶ G⁴³ 2504 R⁵⁶ G⁴⁴ 2505 R⁵⁷ G⁴¹ 2506 R⁵⁷ G⁴² 2507 R⁵⁷ G⁴³ 2508 R⁵⁷ G⁴⁴ 2509 R¹ G⁴⁵ 2510 R¹ G⁴⁶ 2511 R¹ G⁴⁷ 2512 R¹ G⁴⁸ 2513 R² G⁴⁵ 2514 R² G⁴⁶ 2515 R² G⁴⁷ 2516 R² G⁴⁸ 2517 R³ G⁴⁵ 2518 R³ G⁴⁶ 2519 R³ G⁴⁷ 2520 R³ G⁴⁸ 2521 R⁴ G⁴⁵ 2522 R⁴ G⁴⁶ 2523 R⁴ G⁴⁷ 2524 R⁴ G⁴⁸ 2525 R⁵ G⁴⁵ 2526 R⁵ G⁴⁶ 2527 R⁵ G⁴⁷ 2528 R⁵ G⁴⁸ 2529 R⁶ G⁴⁵ 2530 R⁶ G⁴⁶ 2531 R⁶ G⁴⁷ 2532 R⁶ G⁴⁸ 2533 R⁷ G⁴⁵ 2534 R⁷ G⁴⁶ 2535 R⁷ G⁴⁷ 2536 R⁷ G⁴⁸ 2537 R⁸ G⁴⁵ 2538 R⁸ G⁴⁶ 2539 R⁸ G⁴⁷ 2540 R⁸ G⁴⁸ 2541 R⁹ G⁴⁵ 2542 R⁹ G⁴⁶ 2543 R⁹ G⁴⁷ 2544 R⁹ G⁴⁸ 2545 R¹⁰ G⁴⁵ 2546 R¹⁰ G⁴⁶ 2547 R¹⁰ G⁴⁷ 2548 R¹⁰ G⁴⁸ 2549 R¹¹ G⁴⁵ 2550 R¹¹ G⁴⁶ 2551 R¹¹ G⁴⁷ 2552 R¹¹ G⁴⁸ 2553 R¹² G⁴⁵ 2554 R¹² G⁴⁶ 2555 R¹² G⁴⁷ 2556 R¹² G⁴⁸ 2557 R¹³ G⁴⁵ 2558 R¹³ G⁴⁶ 2559 R¹³ G⁴⁷ 2560 R¹³ G⁴⁸ 2561 R¹⁴ G⁴⁵ 2562 R¹⁴ G⁴⁶ 2563 R¹⁴ G⁴⁷ 2564 R¹⁴ G⁴⁸ 2565 R¹⁵ G⁴⁵ 2566 R¹⁵ G⁴⁶ 2567 R¹⁵ G⁴⁷ 2568 R¹⁵ G⁴⁸ 2569 R¹⁶ G⁴⁵ 2570 R¹⁶ G⁴⁶ 2571 R¹⁶ G⁴⁷ 2572 R¹⁶ G⁴⁸ 2573 R¹⁷ G⁴⁵ 2574 R¹⁷ G⁴⁶ 2575 R¹⁷ G⁴⁷ 2576 R¹⁷ G⁴⁸ 2577 R¹⁸ G⁴⁵ 2578 R¹⁸ G⁴⁶ 2579 R¹⁸ G⁴⁷ 2580 R¹⁸ G⁴⁸ 2581 R¹⁹ G⁴⁵ 2582 R¹⁹ G⁴⁶ 2583 R¹⁹ G⁴⁷ 2584 R¹⁹ G⁴⁸ 2585 R²⁰ G⁴⁵ 2586 R²⁰ G⁴⁶ 2587 R²⁰ G⁴⁷ 2588 R²⁰ G⁴⁸ 2589 R²¹ G⁴⁵ 2590 R²¹ G⁴⁶ 2591 R²¹ G⁴⁷ 2592 R²¹ G⁴⁸ 2593 R²² G⁴⁵ 2594 R²² G⁴⁶ 2595 R²² G⁴⁷ 2596 R²² G⁴⁸ 2597 R²³ G⁴⁵ 2598 R²³ G⁴⁶ 2599 R²³ G⁴⁷ 2600 R²³ G⁴⁸ 2601 R²⁴ G⁴⁵ 2602 R²⁴ G⁴⁶ 2603 R²⁴ G⁴⁷ 2604 R²⁴ G⁴⁸ 2605 R²⁵ G⁴⁵ 2606 R²⁵ G⁴⁶ 2607 R²⁵ G⁴⁷ 2608 R²⁵ G⁴⁸ 2609 R²⁶ G⁴⁵ 2610 R²⁶ G⁴⁶ 2611 R²⁶ G⁴⁷ 2612 R²⁶ G⁴⁸ 2613 R²⁷ G⁴⁵ 2614 R²⁷ G⁴⁶ 2615 R²⁷ G⁴⁷ 2616 R²⁷ G⁴⁸ 2617 R²⁸ G⁴⁵ 2618 R²⁸ G⁴⁶ 2619 R²⁸ G⁴⁷ 2620 R²⁸ G⁴⁸ 2621 R²⁹ G⁴⁵ 2622 R²⁹ G⁴⁶ 2623 R²⁹ G⁴⁷ 2624 R²⁹ G⁴⁸ 2625 R³⁰ G⁴⁵ 2626 R³⁰ G⁴⁶ 2627 R³⁰ G⁴⁷ 2628 R³⁰ G⁴⁸ 2629 R³¹ G⁴⁵ 2630 R³¹ G⁴⁶ 2631 R³¹ G⁴⁷ 2632 R³¹ G⁴⁸ 2633 R³² G⁴⁵ 2634 R³² G⁴⁶ 2635 R³² G⁴⁷ 2636 R³² G⁴⁸ 2637 R³³ G⁴⁵ 2638 R³³ G⁴⁶ 2639 R³³ G⁴⁷ 2640 R³³ G⁴⁸ 2641 R³⁴ G⁴⁵ 2642 R³⁴ G⁴⁶ 2643 R³⁴ G⁴⁷ 2644 R³⁴ G⁴⁸ 2645 R³⁵ G⁴⁵ 2646 R³⁵ G⁴⁶ 2647 R³⁵ G⁴⁷ 2648 R³⁵ G⁴⁸ 2649 R³⁶ G⁴⁵ 2650 R³⁶ G⁴⁶ 2651 R³⁶ G⁴⁷ 2652 R³⁶ G⁴⁸ 2653 R³⁷ G⁴⁵ 2654 R³⁷ G⁴⁶ 2655 R³⁷ G⁴⁷ 2656 R³⁷ G⁴⁸ 2657 R³⁸ G⁴⁵ 2658 R³⁸ G⁴⁶ 2659 R³⁸ G⁴⁷ 2660 R³⁸ G⁴⁸ 2661 R³⁹ G⁴⁵ 2662 R³⁹ G⁴⁶ 2663 R³⁹ G⁴⁷ 2664 R³⁹ G⁴⁸ 2665 R⁴⁰ G⁴⁵ 2666 R⁴⁰ G⁴⁶ 2667 R⁴⁰ G⁴⁷ 2668 R⁴⁰ G⁴⁸ 2669 R⁴¹ G⁴⁵ 2670 R⁴¹ G⁴⁶ 2671 R⁴¹ G⁴⁷ 2672 R⁴¹ G⁴⁸ 2673 R⁴² G⁴⁵ 2674 R⁴² G⁴⁶ 2675 R⁴² G⁴⁷ 2676 R⁴² G⁴⁸ 2677 R⁴³ G⁴⁵ 2678 R⁴³ G⁴⁶ 2679 R⁴³ G⁴⁷ 2680 R⁴³ G⁴⁸ 2681 R⁴⁴ G⁴⁵ 2682 R⁴⁴ G⁴⁶ 2683 R⁴⁴ G⁴⁷ 2684 R⁴⁴ G⁴⁸ 2685 R⁴⁵ G⁴⁵ 2686 R⁴⁵ G⁴⁶ 2687 R⁴⁵ G⁴⁷ 2688 R⁴⁵ G⁴⁸ 2689 R⁴⁶ G⁴⁵ 2690 R⁴⁶ G⁴⁶ 2691 R⁴⁶ G⁴⁷ 2692 R⁴⁶ G⁴⁸ 2693 R⁴⁷ G⁴⁵ 2694 R⁴⁷ G⁴⁶ 2695 R⁴⁷ G⁴⁷ 2696 R⁴⁷ G⁴⁸ 2697 R⁴⁸ G⁴⁵ 2698 R⁴⁸ G⁴⁶ 2699 R⁴⁸ G⁴⁷ 2700 R⁴⁸ G⁴⁸ 2701 R⁴⁹ G⁴⁵ 2702 R⁴⁹ G⁴⁶ 2703 R⁴⁹ G⁴⁷ 2704 R⁴⁹ G⁴⁸ 2705 R⁵⁰ G⁴⁵ 2706 R⁵⁰ G⁴⁶ 2707 R⁵⁰ G⁴⁷ 2708 R⁵⁰ G⁴⁸ 2709 R⁵¹ G⁴⁵ 2710 R⁵¹ G⁴⁶ 2711 R⁵¹ G⁴⁷ 2712 R⁵¹ G⁴⁸ 2713 R⁵² G⁴⁵ 2714 R⁵² G⁴⁶ 2715 R⁵² G⁴⁷ 2716 R⁵² G⁴⁸ 2717 R⁵³ G⁴⁵ 2718 R⁵³ G⁴⁶ 2719 R⁵³ G⁴⁷ 2720 R⁵³ G⁴⁸ 2721 R⁵⁴ G⁴⁵ 2722 R⁵⁴ G⁴⁶ 2723 R⁵⁴ G⁴⁷ 2724 R⁵⁴ G⁴⁸ 2725 R⁵⁵ G⁴⁵ 2726 R⁵⁵ G⁴⁶ 2727 R⁵⁵ G⁴⁷ 2728 R⁵⁵ G⁴⁸ 2729 R⁵⁶ G⁴⁵ 2730 R⁵⁶ G⁴⁶ 2731 R⁵⁶ G⁴⁷ 2732 R⁵⁶ G⁴⁸ 2733 R⁵⁷ G⁴⁵ 2734 R⁵⁷ G⁴⁶ 2735 R⁵⁷ G⁴⁷ 2736 R⁵⁷ G⁴⁸ 2737 R¹ G⁴⁹ 2738 R¹ G⁵⁰ 2739 R¹ G⁵¹ 2740 R¹ G⁵² 2741 R² G⁴⁹ 2742 R² G⁵⁰ 2743 R² G⁵¹ 2744 R² G⁵² 2745 R³ G⁴⁹ 2746 R³ G⁵⁰ 2747 R³ G⁵¹ 2748 R³ G⁵² 2749 R⁴ G⁴⁹ 2750 R⁴ G⁵⁰ 2751 R⁴ G⁵¹ 2752 R⁴ G⁵² 2753 R⁵ G⁴⁹ 2754 R⁵ G⁵⁰ 2755 R⁵ G⁵¹ 2756 R⁵ G⁵² 2757 R⁶ G⁴⁹ 2758 R⁶ G⁵⁰ 2759 R⁶ G⁵¹ 2760 R⁶ G⁵² 2761 R⁷ G⁴⁹ 2762 R⁷ G⁵⁰ 2763 R⁷ G⁵¹ 2764 R⁷ G⁵² 2765 R⁸ G⁴⁹ 2766 R⁸ G⁵⁰ 2767 R⁸ G⁵¹ 2768 R⁸ G⁵² 2769 R⁹ G⁴⁹ 2770 R⁹ G⁵⁰ 2771 R⁹ G⁵¹ 2772 R⁹ G⁵² 2773 R¹⁰ G⁴⁹ 2774 R¹⁰ G⁵⁰ 2775 R¹⁰ G⁵¹ 2776 R¹⁰ G⁵² 2777 R¹¹ G⁴⁹ 2778 R¹¹ G⁵⁰ 2779 R¹¹ G⁵¹ 2780 R¹¹ G⁵² 2781 R¹² G⁴⁹ 2782 R¹² G⁵⁰ 2783 R¹² G⁵¹ 2784 R¹² G⁵² 2785 R¹³ G⁴⁹ 2786 R¹³ G⁵⁰ 2787 R¹³ G⁵¹ 2788 R¹³ G⁵² 2789 R¹⁴ G⁴⁹ 2790 R¹⁴ G⁵⁰ 2791 R¹⁴ G⁵¹ 2792 R¹⁴ G⁵² 2793 R¹⁵ G⁴⁹ 2794 R¹⁵ G⁵⁰ 2795 R¹⁵ G⁵¹ 2796 R¹⁵ G⁵² 2797 R¹⁶ G⁴⁹ 2798 R¹⁶ G⁵⁰ 2799 R¹⁶ G⁵¹ 2800 R¹⁶ G⁵² 2801 R¹⁷ G⁴⁹ 2802 R¹⁷ G⁵⁰ 2803 R¹⁷ G⁵¹ 2804 R¹⁷ G⁵² 2805 R¹⁸ G⁴⁹ 2806 R¹⁸ G⁵⁰ 2807 R¹⁸ G⁵¹ 2808 R¹⁸ G⁵² 2809 R¹⁹ G⁴⁹ 2810 R¹⁹ G⁵⁰ 2811 R¹⁹ G⁵¹ 2812 R¹⁹ G⁵² 2813 R²⁰ G⁴⁹ 2814 R²⁰ G⁵⁰ 2815 R²⁰ G⁵¹ 2816 R²⁰ G⁵² 2817 R²¹ G⁴⁹ 2818 R²¹ G⁵⁰ 2819 R²¹ G⁵¹ 2820 R²¹ G⁵² 2821 R²² G⁴⁹ 2822 R²² G⁵⁰ 2823 R²² G⁵¹ 2824 R²² G⁵² 2825 R²³ G⁴⁹ 2826 R²³ G⁵⁰ 2827 R²³ G⁵¹ 2828 R²³ G⁵² 2829 R²⁴ G⁴⁹ 2830 R²⁴ G⁵⁰ 2831 R²⁴ G⁵¹ 2832 R²⁴ G⁵² 2833 R²⁵ G⁴⁹ 2834 R²⁵ G⁵⁰ 2835 R²⁵ G⁵¹ 2836 R²⁵ G⁵² 2837 R²⁶ G⁴⁹ 2838 R²⁶ G⁵⁰ 2839 R²⁶ G⁵¹ 2840 R²⁶ G⁵² 2841 R²⁷ G⁴⁹ 2842 R²⁷ G⁵⁰ 2843 R²⁷ G⁵¹ 2844 R²⁷ G⁵² 2845 R²⁸ G⁴⁹ 2846 R²⁸ G⁵⁰ 2847 R²⁸ G⁵¹ 2848 R²⁸ G⁵² 2849 R²⁹ G⁴⁹ 2850 R²⁹ G⁵⁰ 2851 R²⁹ G⁵¹ 2852 R²⁹ G⁵² 2853 R³⁰ G⁴⁹ 2854 R³⁰ G⁵⁰ 2855 R³⁰ G⁵¹ 2856 R³⁰ G⁵² 2857 R³¹ G⁴⁹ 2858 R³¹ G⁵⁰ 2859 R³¹ G⁵¹ 2860 R³¹ G⁵² 2861 R³² G⁴⁹ 2862 R³² G⁵⁰ 2863 R³² G⁵¹ 2864 R³² G⁵² 2865 R³³ G⁴⁹ 2866 R³³ G⁵⁰ 2867 R³³ G⁵¹ 2868 R³³ G⁵² 2869 R³⁴ G⁴⁹ 2870 R³⁴ G⁵⁰ 2871 R³⁴ G⁵¹ 2872 R³⁴ G⁵² 2873 R³⁵ G⁴⁹ 2874 R³⁵ G⁵⁰ 2875 R³⁵ G⁵¹ 2876 R³⁵ G⁵² 2877 R³⁶ G⁴⁹ 2878 R³⁶ G⁵⁰ 2879 R³⁶ G⁵¹ 2880 R³⁶ G⁵² 2881 R³⁷ G⁴⁹ 2882 R³⁷ G⁵⁰ 2883 R³⁷ G⁵¹ 2884 R³⁷ G⁵² 2885 R³⁸ G⁴⁹ 2886 R³⁸ G⁵⁰ 2887 R³⁸ G⁵¹ 2888 R³⁸ G⁵² 2889 R³⁹ G⁴⁹ 2890 R³⁹ G⁵⁰ 2891 R³⁹ G⁵¹ 2892 R³⁹ G⁵² 2893 R⁴⁰ G⁴⁹ 2894 R⁴⁰ G⁵⁰ 2895 R⁴⁰ G⁵¹ 2896 R⁴⁰ G⁵² 2897 R⁴¹ G⁴⁹ 2898 R⁴¹ G⁵⁰ 2899 R⁴¹ G⁵¹ 2900 R⁴¹ G⁵² 2901 R⁴² G⁴⁹ 2902 R⁴² G⁵⁰ 2903 R⁴² G⁵¹ 2904 R⁴² G⁵² 2905 R⁴³ G⁴⁹ 2906 R⁴³ G⁵⁰ 2907 R⁴³ G⁵¹ 2908 R⁴³ G⁵² 2909 R⁴⁴ G⁴⁹ 2910 R⁴⁴ G⁵⁰ 2911 R⁴⁴ G⁵¹ 2912 R⁴⁴ G⁵² 2913 R⁴⁵ G⁴⁹ 2914 R⁴⁵ G⁵⁰ 2915 R⁴⁵ G⁵¹ 2916 R⁴⁵ G⁵² 2917 R⁴⁶ G⁴⁹ 2918 R⁴⁶ G⁵⁰ 2919 R⁴⁶ G⁵¹ 2920 R⁴⁶ G⁵² 2921 R⁴⁷ G⁴⁹ 2922 R⁴⁷ G⁵⁰ 2923 R⁴⁷ G⁵¹ 2924 R⁴⁷ G⁵² 2925 R⁴⁸ G⁴⁹ 2926 R⁴⁸ G⁵⁰ 2927 R⁴⁸ G⁵¹ 2928 R⁴⁸ G⁵² 2929 R⁴⁹ G⁴⁹ 2930 R⁴⁹ G⁵⁰ 2931 R⁴⁹ G⁵¹ 2932 R⁴⁹ G⁵² 2933 R⁵⁰ G⁴⁹ 2934 R⁵⁰ G⁵⁰ 2935 R⁵⁰ G⁵¹ 2936 R⁵⁰ G⁵² 2937 R⁵¹ G⁴⁹ 2938 R⁵¹ G⁵⁰ 2939 R⁵¹ G⁵¹ 2940 R⁵¹ G⁵² 2941 R⁵² G⁴⁹ 2942 R⁵² G⁵⁰ 2943 R⁵² G⁵¹ 2944 R⁵² G⁵² 2945 R⁵³ G⁴⁹ 2946 R⁵³ G⁵⁰ 2947 R⁵³ G⁵¹ 2948 R⁵³ G⁵² 2949 R⁵⁴ G⁴⁹ 2950 R⁵⁴ G⁵⁰ 2951 R⁵⁴ G⁵¹ 2952 R⁵⁴ G⁵² 2953 R⁵⁵ G⁴⁹ 2954 R⁵⁵ G⁵⁰ 2955 R⁵⁵ G⁵¹ 2956 R⁵⁵ G⁵² 2957 R⁵⁶ G⁴⁹ 2958 R⁵⁶ G⁵⁰ 2959 R⁵⁶ G⁵¹ 2960 R⁵⁶ G⁵² 2961 R⁵⁷ G⁴⁹ 2962 R⁵⁷ G⁵⁰ 2963 R⁵⁷ G⁵¹ 2964 R⁵⁷ G⁵²

where R¹ to R⁵⁷ have the following structures:

wherein G¹ to G⁵² have the following structures:


11. The compound of claim 1, wherein the compound has a formula of M(L_(A))_(p)(L_(B))_(q)(L_(C))_(r), wherein L_(B) and L_(C) are each a bidentate ligand; and wherein p is 1, 2, or 3; q is 0, 1, or 2; r is 0, 1, or 2; and p+q+r is the oxidation state of the metal M.
 12. The compound of claim 11, wherein the compound has a formula selected from the group consisting of Ir(L_(A))₃, Ir(L_(A))(L_(B))₂, Ir(L_(A))₂(L_(B)), Ir(L_(A))₂(L_(C)), and Ir(L_(A))(L_(B))(L_(C)); and wherein L_(A), L_(B), and L_(C) are different from each other; or a formula of Pt(L_(A))(L_(B)); and wherein L_(A) and L_(B) can be same or different.
 13. The compound of claim 11, wherein L_(B) and L_(C) are each independently selected from the group consisting of:

wherein: R_(a)′, R_(b)′, and R_(c)′ each independently represents zero, mono, or up to a maximum allowed number of substitutions to its associated ring; each of R_(a1), R_(b1), R_(c1), R_(a), R_(b), R_(c), R_(N), R_(a)′, R_(b)′, and R_(c)′ is independently hydrogen or a substituent selected from the group consisting of deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, boryl, and combinations thereof; and two adjacent R_(a)′, R_(b)′, and R_(c)′ can be fused or joined to form a ring or form a multidentate ligand.
 14. The compound of claim 12, wherein: when the compound has formula Ir(L_(Ai-m-X))₃, i is an integer from 1 to 2964; m is an integer from 1 to 52; X is an integer from 1 to 4, and the compound is selected from the group consisting of Ir(L_(A1-1-1))₃ to Ir(L_(A2964-52-4))₃; when the compound has formula Ir(L_(Ai-m-X))(L_(Bk))₂, i is an integer from 1 to 2964; m is an integer from 1 to 52; X is an integer from 1 to 4, k is an integer from 1 to 324; and the compound is selected from the group consisting of Ir(L_(A1-1-1))(L_(B1))₂ to Ir(L_(A2964-52-4))(L_(B324))₂; when the compound has formula Ir(L_(Ai-m-X))₂(L_(Bk)), i is an integer from 1 to 2964; m is an integer from 1 to 52; X is an integer from 1 to 4, k is an integer from 1 to 324; and the compound is selected from the group consisting of Ir(L_(A1-1-1))₂(L_(B1)) to Ir(L_(A2964-52-4))₂(L_(B324)); when the compound has formula Ir(L_(Ai-m-X))₂(L_(Cj-I)), i is an integer from 1 to 2964; m is an integer from 1 to 52; X is an integer from 1 to 4, j is an integer from 1 to 1416; and the compound is selected from the group consisting of Ir(L_(A1-1-1))₂(L_(Cj-I)) to Ir(L_(A2964-52-4))₂(L_(C1416-1)); and when the compound has formula Ir(L_(Ai-m-X))₂(L_(Cj-II)), i is an integer from 1 to 2964, m is an integer from 1 to 52; X is an integer from 1 to 4, j is an integer from 1 to 1416; and the compound is selected from the group consisting of Ir(L_(A1-1-1))₂L_(C1-II)) to Ir(L_(A2964-52-4))₂(L_(C1416-II)); wherein each L_(Bk) has the structure defined below:

wherein each L_(Cj-I) has a structure based on formula

and each L_(Cj-II) has a structure based on formula

wherein for each L_(Cj) in L_(Cj-I) and L_(Cj-II), R²⁰¹ and R²⁰² are each independently defined as follows: L_(Cj) R²⁰¹ R²⁰² L_(Cj) R²⁰¹ R²⁰² L_(Cj) R²⁰¹ R²⁰² L_(Cj) R²⁰¹ R²⁰² L_(C1) R^(D1) R^(D1) L_(C193) R^(D1) R^(D3) L_(C385) R^(D17) R^(D40) L_(C577) R^(D143) R^(D120) L_(C2) R^(D2) R^(D2) L_(C194) R^(D1) R^(D4) L_(C386) R^(D17) R^(D41) L_(C578) R^(D143) R^(D133) L_(C3) R^(D3) R^(D3) L_(C195) R^(D1) R^(D5) L_(C387) R^(D17) R^(D42) L_(C579) R^(D143) R^(D134) L_(C4) R^(D4) R^(D4) L_(C196) R^(D1) R^(D9) L_(C388) R^(D17) R^(D43) L_(C580) R^(D143) R^(D135) L_(C5) R^(D5) R^(D5) L_(C197) R^(D1) R^(D10) L_(C389) R^(D17) R^(D48) L_(C581) R^(D143) R^(D136) L_(C6) R^(D6) R^(D6) L_(C198) R^(D1) R^(D17) L_(C390) R^(D17) R^(D49) L_(C582) R^(D143) R^(D144) L_(C7) R^(D7) R^(D7) L_(C199) R^(D1) R^(D18) L_(C391) R^(D17) R^(D50) L_(C583) R^(D143) R^(D145) L_(C8) R^(D8) R^(D8) L_(C200) R^(D1) R^(D20) L_(C392) R^(D17) R^(D54) L_(C584) R^(D143) R^(D146) L_(C9) R^(D9) R^(D9) L_(C201) R^(D1) R^(D22) L_(C393) R^(D17) R^(D55) L_(C585) R^(D143) R^(D147) L_(C10) R^(D10) R^(D10) L_(C202) R^(D1) R^(D37) L_(C394) R^(D17) R^(D58) L_(C586) R^(D143) R^(D149) L_(C11) R^(D11) R^(D11) L_(C203) R^(D1) R^(D40) L_(C395) R^(D17) R^(D59) L_(C587) R^(D143) R^(D151) L_(C12) R^(D12) R^(D12) L_(C204) R^(D1) R^(D41) L_(C396) R^(D17) R^(D78) L_(C588) R^(D143) R^(D154) L_(C13) R^(D13) R^(D13) L_(C205) R^(D1) R^(D42) L_(C397) R^(D17) R^(D79) L_(C589) R^(D143) R^(D155) L_(C14) R^(D14) R^(D14) L_(C206) R^(D1) R^(D43) L_(C398) R^(D17) R^(D81) L_(C590) R^(D143) R^(D161) L_(C15) R^(D15) R^(D15) L_(C207) R^(D1) R^(D48) L_(C399) R^(D17) R^(D87) L_(C591) R^(D143) R^(D175) L_(C16) R^(D16) R^(D16) L_(C208) R^(D1) R^(D49) L_(C400) R^(D17) R^(D88) L_(C592) R^(D144) R^(D3) L_(C17) R^(D17) R^(D17) L_(C209) R^(D1) R^(D50) L_(C401) R^(D17) R^(D89) L_(C593) R^(D144) R^(D5) L_(C18) R^(D18) R^(D18) L_(C210) R^(D1) R^(D54) L_(C402) R^(D17) R^(D93) L_(C594) R^(D144) R^(D17) L_(C19) R^(D19) R^(D19) L_(C211) R^(D1) R^(D55) L_(C403) R^(D17) R^(D116) L_(C595) R^(D144) R^(D18) L_(C20) R^(D20) R^(D20) L_(C212) R^(D1) R^(D58) L_(C404) R^(D17) R^(D117) L_(C596) R^(D144) R^(D20) L_(C21) R^(D21) R^(D21) L_(C213) R^(D1) R^(D59) L_(C405) R^(D17) R^(D118) L_(C597) R^(D144) R^(D22) L_(C22) R^(D22) R^(D22) L_(C214) R^(D1) R^(D78) L_(C406) R^(D17) R^(D119) L_(C598) R^(D144) R^(D37) L_(C23) R^(D23) R^(D23) L_(C215) R^(D1) R^(D79) L_(C407) R^(D17) R^(D120) L_(C599) R^(D144) R^(D40) L_(C24) R^(D24) R^(D24) L_(C216) R^(D1) R^(D81) L_(C408) R^(D17) R^(D133) L_(C600) R^(D144) R^(D41) L_(C25) R^(D25) R^(D25) L_(C217) R^(D1) R^(D87) L_(C409) R^(D17) R^(D134) L_(C601) R^(D144) R^(D42) L_(C26) R^(D26) R^(D26) L_(C218) R^(D1) R^(D88) L_(C410) R^(D17) R^(D135) L_(C602) R^(D144) R^(D43) L_(C27) R^(D27) R^(D27) L_(C219) R^(D1) R^(D89) L_(C411) R^(D17) R^(D136) L_(C603) R^(D144) R^(D48) L_(C28) R^(D28) R^(D28) L_(C220) R^(D1) R^(D93) L_(C412) R^(D17) R^(D143) L_(C604) R^(D144) R^(D49) L_(C29) R^(D29) R^(D29) L_(C221) R^(D1) R^(D116) L_(C413) R^(D17) R^(D144) L_(C605) R^(D144) R^(D54) L_(C30) R^(D30) R^(D30) L_(C222) R^(D1) R^(D117) L_(C414) R^(D17) R^(D145) L_(C606) R^(D144) R^(D58) L_(C31) R^(D31) R^(D31) L_(C223) R^(D1) R^(D118) L_(C415) R^(D17) R^(D146) L_(C607) R^(D144) R^(D59) L_(C32) R^(D32) R^(D32) L_(C224) R^(D1) R^(D119) L_(C416) R^(D17) R^(D147) L_(C608) R^(D144) R^(D78) L_(C33) R^(D33) R^(D33) L_(C225) R^(D1) R^(D120) L_(C417) R^(D17) R^(D149) L_(C609) R^(D144) R^(D79) L_(C34) R^(D34) R^(D34) L_(C226) R^(D1) R^(D133) L_(C418) R^(D17) R^(D151) L_(C610) R^(D144) R^(D81) L_(C35) R^(D35) R^(D35) L_(C227) R^(D1) R^(D134) L_(C419) R^(D17) R^(D154) L_(C611) R^(D144) R^(D87) L_(C36) R^(D36) R^(D36) L_(C228) R^(D1) R^(D135) L_(C420) R^(D17) R^(D155) L_(C612) R^(D144) R^(D88) L_(C37) R^(D37) R^(D37) L_(C229) R^(D1) R^(D136) L_(C421) R^(D17) R^(D161) L_(C613) R^(D144) R^(D89) L_(C38) R^(D38) R^(D38) L_(C230) R^(D1) R^(D143) L_(C422) R^(D17) R^(D175) L_(C614) R^(D144) R^(D93) L_(C39) R^(D39) R^(D39) L_(C231) R^(D1) R^(D144) L_(C423) R^(D50) R^(D3) L_(C615) R^(D144) R^(D116) L_(C10) R^(D40) R^(D40) L_(C232) R^(D1) R^(D145) L_(C424) R^(D50) R^(D5) L_(C616) R^(D144) R^(D117) L_(C41) R^(D41) R^(D41) L_(C233) R^(D1) R^(D146) L_(C425) R^(D50) R^(D18) L_(C617) R^(D144) R^(D118) L_(C42) R^(D42) R^(D42) L_(C234) R^(D1) R^(D147) L_(C426) R^(D50) R^(D20) L_(C618) R^(D144) R^(D119) L_(C43) R^(D43) R^(D43) L_(C235) R^(D1) R^(D149) L_(C427) R^(D50) R^(D22) L_(C619) R^(D144) R^(D120) L_(C44) R^(D44) R^(D44) L_(C236) R^(D1) R^(D151) L_(C428) R^(D50) R^(D37) L_(C620) R^(D144) R^(D133) L_(C45) R^(D45) R^(D45) L_(C237) R^(D1) R^(D154) L_(C429) R^(D50) R^(D40) L_(C621) R^(D144) R^(D134) L_(C46) R^(D46) R^(D46) L_(C238) R^(D1) R^(D155) L_(C430) R^(D50) R^(D41) L_(C622) R^(D144) R^(D135) L_(C47) R^(D47) R^(D47) L_(C239) R^(D1) R^(D161) L_(C431) R^(D50) R^(D42) L_(C623) R^(D144) R^(D136) L_(C48) R^(D48) R^(D48) L_(C240) R^(D1) R^(D175) L_(C432) R^(D50) R^(D43) L_(C624) R^(D144) R^(D145) L_(C49) R^(D49) R^(D49) L_(C241) R^(D4) R^(D3) L_(C433) R^(D50) R^(D48) L_(C625) R^(D144) R^(D146) L_(C50) R^(D50) R^(D50) L_(C242) R^(D4) R^(D5) L_(C434) R^(D50) R^(D49) L_(C626) R^(D144) R^(D147) L_(C51) R^(D51) R^(D51) L_(C243) R^(D4) R^(D9) L_(C435) R^(D50) R^(D54) L_(C627) R^(D144) R^(D149) L_(C52) R^(D52) R^(D52) L_(C244) R^(D4) R^(D10) L_(C436) R^(D50) R^(D55) L_(C628) R^(D144) R^(D151) L_(C53) R^(D55) R^(D55) L_(C245) R^(D4) R^(D17) L_(C437) R^(D50) R^(D58) L_(C629) R^(D144) R^(D154) L_(C54) R^(D54) R^(D54) L_(C246) R^(D4) R^(D18) L_(C438) R^(D50) R^(D59) L_(C630) R^(D144) R^(D155) L_(C55) R^(D55) R^(D55) L_(C247) R^(D4) R^(D20) L_(C439) R^(D50) R^(D78) L_(C631) R^(D144) R^(D161) L_(C56) R^(D56) R^(D56) L_(C248) R^(D4) R^(D22) L_(C440) R^(D50) R^(D79) L_(C632) R^(D144) R^(D175) L_(C57) R^(D57) R^(D57) L_(C249) R^(D4) R^(D37) L_(C441) R^(D50) R^(D81) L_(C633) R^(D145) R^(D3) L_(C58) R^(D58) R^(D58) L_(C250) R^(D4) R^(D40) L_(C442) R^(D50) R^(D87) L_(C634) R^(D145) R^(D5) L_(C59) R^(D59) R^(D59) L_(C251) R^(D4) R^(D41) L_(C443) R^(D50) R^(D88) L_(C635) R^(D145) R^(D17) L_(C60) R^(D60) R^(D60) L_(C252) R^(D4) R^(D42) L_(C444) R^(D50) R^(D89) L_(C636) R^(D145) R^(D18) L_(C61) R^(D61) R^(D61) L_(C253) R^(D4) R^(D43) L_(C445) R^(D50) R^(D93) L_(C637) R^(D145) R^(D20) L_(C62) R^(D62) R^(D62) L_(C254) R^(D4) R^(D48) L_(C446) R^(D50) R^(D116) L_(C638) R^(D145) R^(D22) L_(C63) R^(D63) R^(D63) L_(C255) R^(D4) R^(D49) L_(C447) R^(D50) R^(D117) L_(C639) R^(D145) R^(D37) L_(C64) R^(D64) R^(D64) L_(C256) R^(D4) R^(D50) L_(C448) R^(D50) R^(D118) L_(C640) R^(D145) R^(D40) L_(C65) R^(D65) R^(D65) L_(C257) R^(D4) R^(D54) L_(C449) R^(D50) R^(D119) L_(C641) R^(D145) R^(D41) L_(C66) R^(D66) R^(D66) L_(C258) R^(D4) R^(D55) L_(C450) R^(D50) R^(D120) L_(C642) R^(D145) R^(D42) L_(C67) R^(D67) R^(D67) L_(C259) R^(D4) R^(D58) L_(C451) R^(D50) R^(D133) L_(C643) R^(D145) R^(D43) L_(C68) R^(D68) R^(D68) L_(C260) R^(D4) R^(D59) L_(C452) R^(D50) R^(D134) L_(C644) R^(D145) R^(D48) L_(C69) R^(D69) R^(D69) L_(C261) R^(D4) R^(D78) L_(C453) R^(D50) R^(D135) L_(C645) R^(D145) R^(D49) L_(C70) R^(D70) R^(D70) L_(C262) R^(D4) R^(D79) L_(C454) R^(D50) R^(D136) L_(C646) R^(D145) R^(D54) L_(C71) R^(D71) R^(D71) L_(C263) R^(D4) R^(D81) L_(C455) R^(D50) R^(D143) L_(C647) R^(D145) R^(D58) L_(C72) R^(D72) R^(D72) L_(C264) R^(D4) R^(D87) L_(C456) R^(D50) R^(D144) L_(C648) R^(D145) R^(D59) L_(C73) R^(D73) R^(D73) L_(C265) R^(D4) R^(D88) L_(C457) R^(D50) R^(D145) L_(C649) R^(D145) R^(D78) L_(C74) R^(D74) R^(D74) L_(C266) R^(D4) R^(D89) L_(C458) R^(D50) R^(D146) L_(C650) R^(D145) R^(D79) L_(C75) R^(D75) R^(D75) L_(C267) R^(D4) R^(D93) L_(C459) R^(D50) R^(D147) L_(C651) R^(D145) R^(D81) L_(C76) R^(D76) R^(D76) L_(C268) R^(D4) R^(D116) L_(C460) R^(D50) R^(D149) L_(C652) R^(D145) R^(D87) L_(C77) R^(D77) R^(D77) L_(C269) R^(D4) R^(D117) L_(C461) R^(D50) R^(D151) L_(C653) R^(D145) R^(D88) L_(C78) R^(D78) R^(D78) L_(C270) R^(D4) R^(D118) L_(C462) R^(D50) R^(D154) L_(C654) R^(D145) R^(D89) L_(C79) R^(D79) R^(D79) L_(C271) R^(D4) R^(D119) L_(C463) R^(D50) R^(D155) L_(C655) R^(D145) R^(D93) L_(C80) R^(D80) R^(D80) L_(C272) R^(D4) R^(D120) L_(C464) R^(D50) R^(D161) L_(C656) R^(D145) R^(D116) L_(C81) R^(D81) R^(D81) L_(C273) R^(D4) R^(D133) L_(C465) R^(D50) R^(D175) L_(C657) R^(D145) R^(D117) L_(C82) R^(D82) R^(D82) L_(C274) R^(D4) R^(D134) L_(C466) R^(D55) R^(D3) L_(C658) R^(D145) R^(D118) L_(C83) R^(D83) R^(D83) L_(C275) R^(D4) R^(D135) L_(C467) R^(D55) R^(D5) L_(C659) R^(D145) R^(D119) L_(C84) R^(D84) R^(D84) L_(C276) R^(D4) R^(D136) L_(C468) R^(D55) R^(D18) L_(C660) R^(D145) R^(D120) L_(C85) R^(D85) R^(D85) L_(C277) R^(D4) R^(D143) L_(C469) R^(D55) R^(D20) L_(C661) R^(D145) R^(D133) L_(C86) R^(D86) R^(D86) L_(C278) R^(D4) R^(D144) L_(C470) R^(D55) R^(D22) L_(C662) R^(D145) R^(D134) L_(C87) R^(D87) R^(D87) L_(C279) R^(D4) R^(D145) L_(C471) R^(D55) R^(D37) L_(C663) R^(D145) R^(D135) L_(C88) R^(D88) R^(D88) L_(C280) R^(D4) R^(D146) L_(C472) R^(D55) R^(D40) L_(C664) R^(D145) R^(D136) L_(C89) R^(D89) R^(D89) L_(C281) R^(D4) R^(D147) L_(C473) R^(D55) R^(D41) L_(C665) R^(D145) R^(D146) L_(C90) R^(D90) R^(D90) L_(C282) R^(D4) R^(D149) L_(C474) R^(D55) R^(D42) L_(C666) R^(D145) R^(D147) L_(C91) R^(D91) R^(D91) L_(C283) R^(D4) R^(D151) L_(C475) R^(D55) R^(D43) L_(C667) R^(D145) R^(D149) L_(C92) R^(D92) R^(D92) L_(C284) R^(D4) R^(D154) L_(C476) R^(D55) R^(D48) L_(C668) R^(D145) R^(D151) L_(C93) R^(D93) R^(D93) L_(C285) R^(D4) R^(D155) L_(C477) R^(D55) R^(D49) L_(C669) R^(D145) R^(D154) L_(C94) R^(D94) R^(D94) L_(C286) R^(D4) R^(D161) L_(C478) R^(D55) R^(D54) L_(C670) R^(D145) R^(D155) L_(C95) R^(D95) R^(D95) L_(C287) R^(D4) R^(D175) L_(C479) R^(D55) R^(D58) L_(C671) R^(D145) R^(D161) L_(C96) R^(D96) R^(D96) L_(C288) R^(D9) R^(D3) L_(C480) R^(D55) R^(D59) L_(C672) R^(D145) R^(D175) L_(C97) R^(D97) R^(D97) L_(C289) R^(D9) R^(D5) L_(C481) R^(D55) R^(D78) L_(C673) R^(D146) R^(D3) L_(C98) R^(D98) R^(D98) L_(C290) R^(D9) R^(D10) L_(C482) R^(D55) R^(D79) L_(C674) R^(D146) R^(D5) L_(C99) R^(D99) R^(D99) L_(C291) R^(D9) R^(D17) L_(C483) R^(D55) R^(D81) L_(C675) R^(D146) R^(D17) L_(C100) R^(D100) R^(D100) L_(C292) R^(D9) R^(D18) L_(C484) R^(D55) R^(D87) L_(C676) R^(D146) R^(D18) L_(C101) R^(D101) R^(D101) L_(C293) R^(D9) R^(D20) L_(C485) R^(D55) R^(D88) L_(C677) R^(D146) R^(D20) L_(C102) R^(D102) R^(D102) L_(C294) R^(D9) R^(D22) L_(C486) R^(D55) R^(D89) L_(C678) R^(D146) R^(D22) L_(C103) R^(D103) R^(D103) L_(C295) R^(D9) R^(D37) L_(C487) R^(D55) R^(D93) L_(C679) R^(D146) R^(D37) L_(C104) R^(D104) R^(D104) L_(C296) R^(D9) R^(D40) L_(C488) R^(D55) R^(D116) L_(C680) R^(D146) R^(D40) L_(C105) R^(D105) R^(D105) L_(C297) R^(D9) R^(D41) L_(C489) R^(D55) R^(D117) L_(C681) R^(D146) R^(D41) L_(C106) R^(D106) R^(D106) L_(C298) R^(D9) R^(D42) L_(C490) R^(D55) R^(D118) L_(C682) R^(D146) R^(D42) L_(C107) R^(D107) R^(D107) L_(C299) R^(D9) R^(D43) L_(C491) R^(D55) R^(D119) L_(C683) R^(D146) R^(D43) L_(C108) R^(D108) R^(D108) L_(C300) R^(D9) R^(D48) L_(C492) R^(D55) R^(D120) L_(C684) R^(D146) R^(D48) L_(C109) R^(D109) R^(D109) L_(C301) R^(D9) R^(D49) L_(C493) R^(D55) R^(D133) L_(C685) R^(D146) R^(D49) L_(C110) R^(D110) R^(D110) L_(C302) R^(D9) R^(D50) L_(C494) R^(D55) R^(D134) L_(C686) R^(D146) R^(D54) L_(C111) R^(D111) R^(D111) L_(C303) R^(D9) R^(D54) L_(C495) R^(D55) R^(D135) L_(C687) R^(D146) R^(D58) L_(C112) R^(D112) R^(D112) L_(C304) R^(D9) R^(D55) L_(C496) R^(D55) R^(D136) L_(C688) R^(D146) R^(D59) L_(C113) R^(D113) R^(D113) L_(C305) R^(D9) R^(D58) L_(C497) R^(D55) R^(D143) L_(C689) R^(D146) R^(D78) L_(C114) R^(D114) R^(D114) L_(C306) R^(D9) R^(D59) L_(C498) R^(D55) R^(D144) L_(C690) R^(D146) R^(D79) L_(C115) R^(D115) R^(D115) L_(C307) R^(D9) R^(D78) L_(C499) R^(D55) R^(D145) L_(C691) R^(D146) R^(D81) L_(C116) R^(D116) R^(D116) L_(C308) R^(D9) R^(D79) L_(C500) R^(D55) R^(D146) L_(C692) R^(D146) R^(D87) L_(C117) R^(D117) R^(D117) L_(C309) R^(D9) R^(D81) L_(C501) R^(D55) R^(D147) L_(C693) R^(D146) R^(D88) L_(C118) R^(D118) R^(D118) L_(C310) R^(D9) R^(D87) L_(C502) R^(D55) R^(D149) L_(C694) R^(D146) R^(D89) L_(C119) R^(D119) R^(D119) L_(C311) R^(D9) R^(D88) L_(C503) R^(D55) R^(D151) L_(C695) R^(D146) R^(D93) L_(C120) R^(D120) R^(D120) L_(C312) R^(D9) R^(D89) L_(C504) R^(D55) R^(D154) L_(C696) R^(D146) R^(D117) L_(C121) R^(D121) R^(D121) L_(C313) R^(D9) R^(D93) L_(C505) R^(D55) R^(D155) L_(C697) R^(D146) R^(D118) L_(C122) R^(D122) R^(D122) L_(C314) R^(D9) R^(D116) L_(C506) R^(D55) R^(D161) L_(C698) R^(D146) R^(D119) L_(C123) R^(D123) R^(D123) L_(C315) R^(D9) R^(D117) L_(C507) R^(D55) R^(D175) L_(C699) R^(D146) R^(D120) L_(C124) R^(D124) R^(D124) L_(C316) R^(D9) R^(D118) L_(C508) R^(D116) R^(D3) L_(C700) R^(D146) R^(D133) L_(C125) R^(D125) R^(D125) L_(C317) R^(D9) R^(D119) L_(C509) R^(D116) R^(D5) L_(C701) R^(D146) R^(D134) L_(C126) R^(D126) R^(D126) L_(C318) R^(D9) R^(D120) L_(C510) R^(D116) R^(D17) L_(C702) R^(D146) R^(D135) L_(C127) R^(D127) R^(D127) L_(C319) R^(D9) R^(D133) L_(C511) R^(D116) R^(D18) L_(C703) R^(D146) R^(D136) L_(C128) R^(D128) R^(D128) L_(C320) R^(D9) R^(D134) L_(C512) R^(D116) R^(D20) L_(C704) R^(D146) R^(D146) L_(C129) R^(D129) R^(D129) L_(C321) R^(D9) R^(D135) L_(C513) R^(D116) R^(D22) L_(C705) R^(D146) R^(D147) L_(C130) R^(D130) R^(D130) L_(C322) R^(D9) R^(D136) L_(C514) R^(D116) R^(D37) L_(C706) R^(D146) R^(D149) L_(C131) R^(D131) R^(D131) L_(C323) R^(D9) R^(D143) L_(C515) R^(D116) R^(D40) L_(C707) R^(D146) R^(D151) L_(C132) R^(D132) R^(D132) L_(C324) R^(D9) R^(D144) L_(C516) R^(D116) R^(D41) L_(C708) R^(D146) R^(D154) L_(C133) R^(D133) R^(D133) L_(C325) R^(D9) R^(D145) L_(C517) R^(D116) R^(D42) L_(C709) R^(D146) R^(D155) L_(C134) R^(D134) R^(D134) L_(C326) R^(D9) R^(D146) L_(C518) R^(D116) R^(D43) L_(C710) R^(D146) R^(D161) L_(C135) R^(D135) R^(D135) L_(C327) R^(D9) R^(D147) L_(C519) R^(D116) R^(D48) L_(C711) R^(D146) R^(D175) L_(C136) R^(D136) R^(D136) L_(C328) R^(D9) R^(D149) L_(C520) R^(D116) R^(D49) L_(C712) R^(D133) R^(D3) L_(C137) R^(D137) R^(D137) L_(C329) R^(D9) R^(D151) L_(C521) R^(D116) R^(D54) L_(C713) R^(D133) R^(D5) L_(C138) R^(D138) R^(D138) L_(C330) R^(D9) R^(D154) L_(C522) R^(D116) R^(D58) L_(C714) R^(D133) R^(D3) L_(C139) R^(D139) R^(D139) L_(C331) R^(D9) R^(D155) L_(C523) R^(D116) R^(D59) L_(C715) R^(D133) R^(D18) L_(C140) R^(D140) R^(D140) L_(C332) R^(D9) R^(D161) L_(C524) R^(D116) R^(D78) L_(C716) R^(D133) R^(D20) L_(C141) R^(D141) R^(D141) L_(C333) R^(D9) R^(D175) L_(C525) R^(D116) R^(D79) L_(C717) R^(D133) R^(D22) L_(C142) R^(D142) R^(D142) L_(C334) R^(D10) R^(D3) L_(C526) R^(D116) R^(D81) L_(C718) R^(D133) R^(D37) L_(C143) R^(D143) R^(D143) L_(C335) R^(D10) R^(D5) L_(C527) R^(D116) R^(D87) L_(C719) R^(D133) R^(D40) L_(C144) R^(D144) R^(D144) L_(C336) R^(D10) R^(D17) L_(C528) R^(D116) R^(D88) L_(C720) R^(D133) R^(D41) L_(C145) R^(D145) R^(D145) L_(C337) R^(D10) R^(D18) L_(C529) R^(D116) R^(D89) L_(C721) R^(D133) R^(D42) L_(C146) R^(D146) R^(D146) L_(C338) R^(D10) R^(D20) L_(C530) R^(D116) R^(D95) L_(C722) R^(D133) R^(D43) L_(C147) R^(D147) R^(D147) L_(C339) R^(D10) R^(D22) L_(C531) R^(D116) R^(D117) L_(C723) R^(D133) R^(D48) L_(C148) R^(D148) R^(D148) L_(C340) R^(D10) R^(D37) L_(C532) R^(D116) R^(D118) L_(C724) R^(D133) R^(D49) L_(C149) R^(D149) R^(D149) L_(C341) R^(D10) R^(D40) L_(C533) R^(D116) R^(D119) L_(C725) R^(D133) R^(D54) L_(C150) R^(D150) R^(D150) L_(C342) R^(D10) R^(D41) L_(C534) R^(D116) R^(D120) L_(C726) R^(D133) R^(D58) L_(C151) R^(D151) R^(D151) L_(C343) R^(D10) R^(D42) L_(C535) R^(D116) R^(D133) L_(C727) R^(D133) R^(D59) L_(C152) R^(D152) R^(D152) L_(C344) R^(D10) R^(D43) L_(C536) R^(D116) R^(D134) L_(C728) R^(D133) R^(D78) L_(C153) R^(D153) R^(D153) L_(C345) R^(D10) R^(D48) L_(C537) R^(D116) R^(D135) L_(C729) R^(D133) R^(D79) L_(C154) R^(D154) R^(D154) L_(C346) R^(D10) R^(D49) L_(C538) R^(D116) R^(D136) L_(C730) R^(D133) R^(D81) L_(C155) R^(D155) R^(D155) L_(C347) R^(D10) R^(D50) L_(C539) R^(D116) R^(D143) L_(C731) R^(D133) R^(D87) L_(C156) R^(D 156) R^(D156) L_(C348) R^(D10) R^(D54) L_(C540) R^(D116) R^(D144) L_(C732) R^(D133) R^(D88) L_(C157) R^(D157) R^(D157) L_(C349) R^(D10) R^(D55) L_(C541) R^(D116) R^(D145) L_(C733) R^(D133) R^(D89) L_(C158) R^(D158) R^(D158) L_(C350) R^(D10) R^(D58) L_(C542) R^(D116) R^(D146) L_(C734) R^(D133) R^(D93) L_(C159) R^(D159) R^(D159) L_(C351) R^(D10) R^(D59) L_(C543) R^(D116) R^(D147) L_(C735) R^(D133) R^(D117) L_(C160) R^(D160) R^(D160) L_(C352) R^(D10) R^(D78) L_(C544) R^(D116) R^(D149) L_(C736) R^(D133) R^(D118) L_(C161) R^(D161) R^(D161) L_(C353) R^(D10) R^(D79) L_(C545) R^(D116) R^(D151) L_(C737) R^(D133) R^(D119) L_(C162) R^(D162) R^(D162) L_(C354) R^(D10) R^(D81) L_(C546) R^(D116) R^(D154) L_(C738) R^(D133) R^(D120) L_(C163) R^(D163) R^(D163) L_(C355) R^(D10) R^(D87) L_(C547) R^(D116) R^(D155) L_(C739) R^(D133) R^(D133) L_(C164) R^(D164) R^(D164) L_(C356) R^(D10) R^(D88) L_(C548) R^(D116) R^(D161) L_(C740) R^(D133) R^(D134) L_(C165) R^(D165) R^(D165) L_(C357) R^(D10) R^(D89) L_(C549) R^(D116) R^(D175) L_(C741) R^(D133) R^(D135) L_(C166) R^(D166) R^(D166) L_(C358) R^(D10) R^(D93) L_(C550) R^(D143) R^(D3) L_(C742) R^(D133) R^(D136) L_(C167) R^(D167) R^(D167) L_(C359) R^(D10) R^(D116) L_(C551) R^(D143) R^(D5) L_(C743) R^(D133) R^(D146) L_(C168) R^(D168) R^(D168) L_(C360) R^(D10) R^(D117) L_(C552) R^(D143) R^(D17) L_(C744) R^(D133) R^(D147) L_(C169) R^(D169) R^(D169) L_(C361) R^(D10) R^(D118) L_(C553) R^(D143) R^(D18) L_(C745) R^(D133) R^(D149) L_(C170) R^(D170) R^(D170) L_(C362) R^(D10) R^(D119) L_(C554) R^(D143) R^(D20) L_(C746) R^(D133) R^(D151) L_(C171) R^(D171) R^(D171) L_(C363) R^(D10) R^(D120) L_(C555) R^(D143) R^(D22) L_(C747) R^(D133) R^(D154) L_(C172) R^(D172) R^(D172) L_(C364) R^(D10) R^(D133) L_(C556) R^(D143) R^(D37) L_(C748) R^(D133) R^(D155) L_(C173) R^(D173) R^(D173) L_(C365) R^(D10) R^(D134) L_(C557) R^(D143) R^(D40) L_(C749) R^(D133) R^(D161) L_(C174) R^(D174) R^(D174) L_(C366) R^(D10) R^(D135) L_(C558) R^(D143) R^(D41) L_(C750) R^(D133) R^(D175) L_(C175) R^(D175) R^(D175) L_(C367) R^(D10) R^(D136) L_(C559) R^(D143) R^(D42) L_(C751) R^(D175) R^(D3) L_(C176) R^(D176) R^(D176) L_(C368) R^(D10) R^(D143) L_(C560) R^(D143) R^(D43) L_(C752) R^(D175) R^(D5) L_(C177) R^(D177) R^(D177) L_(C369) R^(D10) R^(D144) L_(C561) R^(D143) R^(D48) L_(C753) R^(D175) R^(D18) L_(C178) R^(D178) R^(D178) L_(C370) R^(D10) R^(D145) L_(C562) R^(D143) R^(D49) L_(C754) R^(D175) R^(D20) L_(C179) R^(D179) R^(D179) L_(C371) R^(D10) R^(D146) L_(C563) R^(D143) R^(D54) L_(C755) R^(D175) R^(D22) L_(C180) R^(D180) R^(D180) L_(C372) R^(D10) R^(D147) L_(C564) R^(D143) R^(D58) L_(C756) R^(D175) R^(D37) L_(C181) R^(D181) R^(D181) L_(C373) R^(D10) R^(D149) L_(C565) R^(D143) R^(D59) L_(C757) R^(D175) R^(D40) L_(C182) R^(D182) R^(D182) L_(C374) R^(D10) R^(D151) L_(C566) R^(D143) R^(D78) L_(C758) R^(D175) R^(D41) L_(C183) R^(D183) R^(D183) L_(C375) R^(D10) R^(D154) L_(C567) R^(D143) R^(D79) L_(C759) R^(D175) R^(D42) L_(C184) R^(D184) R^(D184) L_(C376) R^(D10) R^(D155) L_(C568) R^(D143) R^(D81) L_(C760) R^(D175) R^(D43) L_(C185) R^(D185) R^(D185) L_(C377) R^(D10) R^(D161) L_(C569) R^(D143) R^(D87) L_(C761) R^(D175) R^(D48) L_(C186) R^(D186) R^(D186) L_(C378) R^(D10) R^(D175) L_(C570) R^(D143) R^(D88) L_(C762) R^(D175) R^(D49) L_(C187) R^(D187) R^(D187) L_(C379) R^(D17) R^(D3) L_(C571) R^(D143) R^(D89) L_(C763) R^(D175) R^(D54) L_(C188) R^(D188) R^(D188) L_(C380) R^(D17) R^(D5) L_(C572) R^(D143) R^(D93) L_(C764) R^(D175) R^(D58) L_(C189) R^(D189) R^(D189) L_(C381) R^(D17) R^(D18) L_(C573) R^(D143) R^(D116) L_(C765) R^(D175) R^(D59) L_(C190) R^(D190) R^(D190) L_(C382) R^(D17) R^(D20) L_(C574) R^(D143) R^(D117) L_(C766) R^(D175) R^(D78) L_(C191) R^(D191) R^(D191) L_(C383) R^(D17) R^(D22) L_(C575) R^(D143) R^(D118) L_(C767) R^(D175) R^(D79) L_(C192) R^(D192) R^(D192) L_(C384) R^(D17) R^(D37) L_(C576) R^(D143) R^(D119) L_(C768) R^(D175) R^(D81) L_(C769) R^(D193) R^(D193) L_(C877) R^(D1) R^(D193) L_(C985) R^(D4) R^(D193) L_(C1093) R^(D9) R^(D193) L_(C770) R^(D194) R^(D194) L_(C878) R^(D1) R^(D194) L_(C986) R^(D4) R^(D194) L_(C1094) R^(D9) R^(D194) L_(C771) R^(D195) R^(D195) L_(C879) R^(D1) R^(D195) L_(C987) R^(D4) R^(D195) L_(C1095) R^(D9) R^(D195) L_(C772) R^(D196) R^(D196) L_(C880) R^(D1) R^(D196) L_(C988) R^(D4) R^(D196) L_(C1096) R^(D9) R^(D196) L_(C773) R^(D197) R^(D197) L_(C881) R^(D1) R^(D197) L_(C989) R^(D4) R^(D197) L_(C1097) R^(D9) R^(D197) L_(C774) R^(D198) R^(D198) L_(C882) R^(D1) R^(D198) L_(C990) R^(D4) R^(D198) L_(C1098) R^(D9) R^(D198) L_(C775) R^(D199) R^(D199) L_(C883) R^(D1) R^(D199) L_(C991) R^(D4) R^(D199) L_(C1099) R^(D9) R^(D199) L_(C776) R^(D200) R^(D200) L_(C884) R^(D1) R^(D200) L_(C992) R^(D4) R^(D200) L_(C1100) R^(D9) R^(D200) L_(C777) R^(D201) R^(D201) L_(C885) R^(D1) R^(D201) L_(C993) R^(D4) R^(D201) L_(C1101) R^(D9) R^(D201) L_(C778) R^(D202) R^(D202) L_(C886) R^(D1) R^(D202) L_(C994) R^(D4) R^(D202) L_(C1102) R^(D9) R^(D202) L_(C779) R^(D203) R^(D203) L_(C887) R^(D1) R^(D203) L_(C995) R^(D4) R^(D203) L_(C1103) R^(D9) R^(D203) L_(C780) R^(D204) R^(D204) L_(C888) R^(D1) R^(D204) L_(C996) R^(D4) R^(D204) L_(C1104) R^(D9) R^(D204) L_(C781) R^(D205) R^(D205) L_(C889) R^(D1) R^(D205) L_(C997) R^(D4) R^(D205) L_(C1105) R^(D9) R^(D205) L_(C782) R^(D206) R^(D206) L_(C890) R^(D1) R^(D206) L_(C998) R^(D4) R^(D206) L_(C1106) R^(D9) R^(D206) L_(C783) R^(D207) R^(D207) L_(C891) R^(D1) R^(D207) L_(C999) R^(D4) R^(D207) L_(C1107) R^(D9) R^(D207) L_(C784) R^(D208) R^(D208) L_(C892) R^(D1) R^(D208) L_(C1000) R^(D4) R^(D208) L_(C1108) R^(D9) R^(D208) L_(C785) R^(D209) R^(D209) L_(C893) R^(D1) R^(D209) L_(C1001) R^(D4) R^(D209) L_(C1109) R^(D9) R^(D209) L_(C786) R^(D210) R^(D210) L_(C894) R^(D1) R^(D210) L_(C1002) R^(D4) R^(D210) L_(C1110) R^(D9) R^(D210) L_(C787) R^(D211) R^(D211) L_(C895) R^(D1) R^(D211) L_(C1003) R^(D4) R^(D211) L_(C1111) R^(D9) R^(D211) L_(C788) R^(D212) R^(D212) L_(C896) R^(D1) R^(D212) L_(C1004) R^(D4) R^(D212) L_(C1112) R^(D9) R^(D212) L_(C789) R^(D213) R^(D213) L_(C897) R^(D1) R^(D213) L_(C1005) R^(D4) R^(D213) L_(C1113) R^(D9) R^(D213) L_(C790) R^(D214) R^(D214) L_(C898) R^(D1) R^(D214) L_(C1006) R^(D4) R^(D214) L_(C1114) R^(D9) R^(D214) L_(C791) R^(D215) R^(D215) L_(C899) R^(D1) R^(D215) L_(C1007) R^(D4) R^(D215) L_(C1115) R^(D9) R^(D215) L_(C792) R^(D216) R^(D216) L_(C900) R^(D1) R^(D216) L_(C1008) R^(D4) R^(D216) L_(C1116) R^(D9) R^(D216) L_(C793) R^(D217) R^(D217) L_(C901) R^(D1) R^(D217) L_(C1009) R^(D4) R^(D217) L_(C1117) R^(D9) R^(D217) L_(C794) R^(D218) R^(D218) L_(C902) R^(D1) R^(D218) L_(C1010) R^(D4) R^(D218) L_(C1118) R^(D9) R^(D218) L_(C795) R^(D219) R^(D219) L_(C903) R^(D1) R^(D219) L_(C1011) R^(D4) R^(D219) L_(C1119) R^(D9) R^(D219) L_(C796) R^(D220) R^(D220) L_(C904) R^(D1) R^(D220) L_(C1012) R^(D4) R^(D220) L_(C1120) R^(D9) R^(D220) L_(C797) R^(D221) R^(D221) L_(C905) R^(D1) R^(D221) L_(C1013) R^(D4) R^(D221) L_(C1121) R^(D9) R^(D221) L_(C798) R^(D222) R^(D222) L_(C906) R^(D1) R^(D222) L_(C1014) R^(D4) R^(D222) L_(C1122) R^(D9) R^(D222) L_(C799) R^(D223) R^(D223) L_(C907) R^(D1) R^(D223) L_(C1015) R^(D4) R^(D223) L_(C1123) R^(D9) R^(D223) L_(C800) R^(D224) R^(D224) L_(C908) R^(D1) R^(D224) L_(C1016) R^(D4) R^(D224) L_(C1124) R^(D9) R^(D224) L_(C801) R^(D225) R^(D225) L_(C909) R^(D1) R^(D225) L_(C1017) R^(D4) R^(D225) L_(C1125) R^(D9) R^(D225) L_(C802) R^(D226) R^(D226) L_(C910) R^(D1) R^(D226) L_(C1018) R^(D4) R^(D226) L_(C1126) R^(D9) R^(D226) L_(C803) R^(D227) R^(D227) L_(C911) R^(D1) R^(D227) L_(C1019) R^(D4) R^(D227) L_(C1127) R^(D9) R^(D227) L_(C804) R^(D228) R^(D228) L_(C912) R^(D1) R^(D228) L_(C1020) R^(D4) R^(D228) L_(C1128) R^(D9) R^(D228) L_(C805) R^(D229) R^(D229) L_(C913) R^(D1) R^(D229) L_(C1021) R^(D4) R^(D229) L_(C1129) R^(D9) R^(D229) L_(C806) R^(D230) R^(D230) L_(C914) R^(D1) R^(D230) L_(C1022) R^(D4) R^(D230) L_(C1130) R^(D9) R^(D230) L_(C807) R^(D231) R^(D231) L_(C915) R^(D1) R^(D231) L_(C1023) R^(D4) R^(D231) L_(C1131) R^(D9) R^(D231) L_(C808) R^(D232) R^(D232) L_(C916) R^(D1) R^(D232) L_(C1024) R^(D4) R^(D232) L_(C1132) R^(D9) R^(D232) L_(C809) R^(D233) R^(D233) L_(C917) R^(D1) R^(D233) L_(C1025) R^(D4) R^(D233) L_(C1133) R^(D9) R^(D233) L_(C810) R^(D234) R^(D234) L_(C918) R^(D1) R^(D234) L_(C1026) R^(D4) R^(D234) L_(C1134) R^(D9) R^(D234) L_(C811) R^(D235) R^(D235) L_(C919) R^(D1) R^(D235) L_(C1027) R^(D4) R^(D235) L_(C1135) R^(D9) R^(D235) L_(C812) R^(D236) R^(D236) L_(C920) R^(D1) R^(D236) L_(C1028) R^(D4) R^(D236) L_(C1136) R^(D9) R^(D236) L_(C813) R^(D237) R^(D237) L_(C921) R^(D1) R^(D237) L_(C1029) R^(D4) R^(D237) L_(C1137) R^(D9) R^(D237) L_(C814) R^(D238) R^(D238) L_(C922) R^(D1) R^(D238) L_(C1030) R^(D4) R^(D238) L_(C1138) R^(D9) R^(D238) L_(C815) R^(D239) R^(D239) L_(C923) R^(D1) R^(D239) L_(C1031) R^(D4) R^(D239) L_(C1139) R^(D9) R^(D239) L_(C816) R^(D240) R^(D240) L_(C924) R^(D1) R^(D240) L_(C1032) R^(D4) R^(D240) L_(C1140) R^(D9) R^(D240) L_(C817) R^(D241) R^(D241) L_(C925) R^(D1) R^(D241) L_(C1033) R^(D4) R^(D241) L_(C1141) R^(D9) R^(D241) L_(C818) R^(D242) R^(D242) L_(C926) R^(D1) R^(D242) L_(C1034) R^(D4) R^(D242) L_(C1142) R^(D9) R^(D242) L_(C819) R^(D243) R^(D243) L_(C927) R^(D1) R^(D243) L_(C1035) R^(D4) R^(D243) L_(C1143) R^(D9) R^(D243) L_(C820) R^(D244) R^(D244) L_(C928) R^(D1) R^(D244) L_(C1036) R^(D4) R^(D244) L_(C1144) R^(D9) R^(D244) L_(C821) R^(D245) R^(D245) L_(C929) R^(D1) R^(D245) L_(C1037) R^(D4) R^(D245) L_(C1145) R^(D9) R^(D245) L_(C822) R^(D246) R^(D246) L_(C930) R^(D1) R^(D246) L_(C1038) R^(D4) R^(D246) L_(C1146) R^(D9) R^(D246) L_(C823) R^(D17) R^(D193) L_(C931) R^(D50) R^(D193) L_(C1039) R^(D145) R^(D193) L_(C1147) R^(D168) R^(D193) L_(C824) R^(D17) R^(D194) L_(C932) R^(D50) R^(D194) L_(C1040) R^(D145) R^(D194) L_(C1148) R^(D168) R^(D194) L_(C825) R^(D17) R^(D195) L_(C933) R^(D50) R^(D195) L_(C1041) R^(D145) R^(D195) L_(C1149) R^(D168) R^(D195) L_(C826) R^(D17) R^(D196) L_(C934) R^(D50) R^(D196) L_(C1042) R^(D145) R^(D196) L_(C1150) R^(D168) R^(D196) L_(C827) R^(D17) R^(D197) L_(C935) R^(D50) R^(D197) L_(C1043) R^(D145) R^(D197) L_(C1151) R^(D168) R^(D197) L_(C828) R^(D17) R^(D198) L_(C936) R^(D50) R^(D198) L_(C1044) R^(D145) R^(D198) L_(C1152) R^(D168) R^(D198) L_(C829) R^(D17) R^(D199) L_(C937) R^(D50) R^(D199) L_(C1045) R^(D145) R^(D199) L_(C1153) R^(D168) R^(D199) L_(C830) R^(D17) R^(D200) L_(C938) R^(D50) R^(D200) L_(C1046) R^(D145) R^(D200) L_(C1154) R^(D168) R^(D200) L_(C831) R^(D17) R^(D201) L_(C939) R^(D50) R^(D201) L_(C1047) R^(D145) R^(D201) L_(C1155) R^(D168) R^(D201) L_(C832) R^(D17) R^(D202) L_(C940) R^(D50) R^(D202) L_(C1048) R^(D145) R^(D202) L_(C1156) R^(D168) R^(D202) L_(C833) R^(D17) R^(D203) L_(C941) R^(D50) R^(D203) L_(C1049) R^(D145) R^(D203) L_(C1157) R^(D168) R^(D203) L_(C834) R^(D17) R^(D204) L_(C942) R^(D50) R^(D204) L_(C1050) R^(D145) R^(D204) L_(C1158) R^(D168) R^(D204) L_(C835) R^(D17) R^(D205) L_(C943) R^(D50) R^(D205) L_(C1051) R^(D145) R^(D205) L_(C1159) R^(D168) R^(D205) L_(C836) R^(D17) R^(D206) L_(C944) R^(D50) R^(D206) L_(C1052) R^(D145) R^(D206) L_(C1160) R^(D168) R^(D206) L_(C837) R^(D17) R^(D207) L_(C945) R^(D50) R^(D207) L_(C1053) R^(D145) R^(D207) L_(C1161) R^(D168) R^(D207) L_(C838) R^(D17) R^(D208) L_(C946) R^(D50) R^(D208) L_(C1054) R^(D145) R^(D208) L_(C1162) R^(D168) R^(D208) L_(C839) R^(D17) R^(D209) L_(C947) R^(D50) R^(D209) L_(C1055) R^(D145) R^(D209) L_(C1163) R^(D168) R^(D209) L_(C840) R^(D17) R^(D210) L_(C948) R^(D50) R^(D210) L_(C1056) R^(D145) R^(D210) L_(C1164) R^(D168) R^(D210) L_(C841) R^(D17) R^(D211) L_(C949) R^(D50) R^(D211) L_(C1057) R^(D145) R^(D211) L_(C1165) R^(D168) R^(D211) L_(C842) R^(D17) R^(D212) L_(C950) R^(D50) R^(D212) L_(C1058) R^(D145) R^(D212) L_(C1166) R^(D168) R^(D212) L_(C843) R^(D17) R^(D213) L_(C951) R^(D50) R^(D213) L_(C1059) R^(D145) R^(D213) L_(C1167) R^(D168) R^(D213) L_(C844) R^(D17) R^(D214) L_(C952) R^(D50) R^(D214) L_(C1060) R^(D145) R^(D214) L_(C1168) R^(D168) R^(D214) L_(C845) R^(D17) R^(D215) L_(C953) R^(D50) R^(D215) L_(C1061) R^(D145) R^(D215) L_(C1169) R^(D168) R^(D215) L_(C846) R^(D17) R^(D216) L_(C954) R^(D50) R^(D216) L_(C1062) R^(D145) R^(D216) L_(C1170) R^(D168) R^(D216) L_(C847) R^(D17) R^(D217) L_(C955) R^(D50) R^(D217) L_(C1063) R^(D145) R^(D217) L_(C1171) R^(D168) R^(D217) L_(C848) R^(D17) R^(D218) L_(C956) R^(D50) R^(D218) L_(C1064) R^(D145) R^(D218) L_(C1172) R^(D168) R^(D218) L_(C849) R^(D17) R^(D219) L_(C957) R^(D50) R^(D219) L_(C1065) R^(D145) R^(D219) L_(C1173) R^(D168) R^(D219) L_(C850) R^(D17) R^(D220) L_(C958) R^(D50) R^(D220) L_(C1066) R^(D145) R^(D220) L_(C1174) R^(D168) R^(D220) L_(C851) R^(D17) R^(D221) L_(C959) R^(D50) R^(D221) L_(C1067) R^(D145) R^(D221) L_(C1175) R^(D168) R^(D221) L_(C852) R^(D17) R^(D222) L_(C960) R^(D50) R^(D222) L_(C1068) R^(D145) R^(D222) L_(C1176) R^(D168) R^(D222) L_(C853) R^(D17) R^(D223) L_(C961) R^(D50) R^(D223) L_(C1069) R^(D145) R^(D223) L_(C1177) R^(D168) R^(D223) L_(C854) R^(D17) R^(D224) L_(C962) R^(D50) R^(D224) L_(C1070) R^(D145) R^(D224) L_(C1178) R^(D168) R^(D224) L_(C855) R^(D17) R^(D225) L_(C963) R^(D50) R^(D225) L_(C1071) R^(D145) R^(D225) L_(C1179) R^(D168) R^(D225) L_(C856) R^(D17) R^(D226) L_(C964) R^(D50) R^(D226) L_(C1072) R^(D145) R^(D226) L_(C1180) R^(D168) R^(D226) L_(C857) R^(D17) R^(D227) L_(C965) R^(D50) R^(D227) L_(C1073) R^(D145) R^(D227) L_(C1181) R^(D168) R^(D227) L_(C858) R^(D17) R^(D228) L_(C966) R^(D50) R^(D228) L_(C1074) R^(D145) R^(D228) L_(C1182) R^(D168) R^(D228) L_(C859) R^(D17) R^(D229) L_(C967) R^(D50) R^(D229) L_(C1075) R^(D145) R^(D229) L_(C1183) R^(D168) R^(D229) L_(C860) R^(D17) R^(D230) L_(C968) R^(D50) R^(D230) L_(C1076) R^(D145) R^(D230) L_(C1184) R^(D168) R^(D230) L_(C861) R^(D17) R^(D231) L_(C969) R^(D50) R^(D231) L_(C1077) R^(D145) R^(D231) L_(C1185) R^(D168) R^(D231) L_(C862) R^(D17) R^(D232) L_(C970) R^(D50) R^(D232) L_(C1078) R^(D145) R^(D232) L_(C1186) R^(D168) R^(D232) L_(C863) R^(D17) R^(D233) L_(C971) R^(D50) R^(D233) L_(C1079) R^(D145) R^(D233) L_(C1187) R^(D168) R^(D233) L_(C864) R^(D17) R^(D234) L_(C972) R^(D50) R^(D234) L_(C1080) R^(D145) R^(D234) L_(C1188) R^(D168) R^(D234) L_(C865) R^(D17) R^(D235) L_(C973) R^(D50) R^(D235) L_(C1081) R^(D145) R^(D235) L_(C1189) R^(D168) R^(D235) L_(C866) R^(D17) R^(D236) L_(C974) R^(D50) R^(D236) L_(C1082) R^(D145) R^(D236) L_(C1190) R^(D168) R^(D236) L_(C867) R^(D17) R^(D237) L_(C975) R^(D50) R^(D237) L_(C1083) R^(D145) R^(D237) L_(C1191) R^(D168) R^(D237) L_(C868) R^(D17) R^(D238) L_(C976) R^(D50) R^(D238) L_(C1084) R^(D145) R^(D238) L_(C1192) R^(D168) R^(D238) L_(C869) R^(D17) R^(D239) L_(C977) R^(D50) R^(D239) L_(C1085) R^(D145) R^(D239) L_(C1193) R^(D168) R^(D239) L_(C870) R^(D17) R^(D240) L_(C978) R^(D50) R^(D240) L_(C1086) R^(D145) R^(D240) L_(C1194) R^(D168) R^(D240) L_(C871) R^(D17) R^(D241) L_(C979) R^(D50) R^(D241) L_(C1087) R^(D145) R^(D241) L_(C1195) R^(D168) R^(D241) L_(C872) R^(D17) R^(D242) L_(C980) R^(D50) R^(D242) L_(C1088) R^(D145) R^(D242) L_(C1196) R^(D168) R^(D242) L_(C873) R^(D17) R^(D243) L_(C981) R^(D50) R^(D243) L_(C1089) R^(D145) R^(D243) L_(C1197) R^(D168) R^(D243) L_(C874) R^(D17) R^(D244) L_(C982) R^(D50) R^(D244) L_(C1090) R^(D145) R^(D244) L_(C1198) R^(D168) R^(D244) L_(C875) R^(D17) R^(D245) L_(C983) R^(D50) R^(D245) L_(C1091) R^(D145) R^(D245) L_(C1199) R^(D168) R^(D245) L_(C876) R^(D17) R^(D246) L_(C984) R^(D50) R^(D246) L_(C1092) R^(D145) R^(D246) L_(C1200) R^(D168) R^(D246) L_(C1201) R^(D10) R^(D193) L_(C1255) R^(D55) R^(D193) L_(C1309) R^(D37) R^(D193) L_(C1363) R^(D143) R^(D193) L_(C1202) R^(D10) R^(D194) L_(C1256) R^(D55) R^(D194) L_(C1310) R^(D37) R^(D194) L_(C1364) R^(D143) R^(D194) L_(C1203) R^(D10) R^(D195) L_(C1257) R^(D55) R^(D195) L_(C1311) R^(D37) R^(D195) L_(C1365) R^(D143) R^(D195) L_(C1204) R^(D10) R^(D196) L_(C1258) R^(D55) R^(D196) L_(C1312) R^(D37) R^(D196) L_(C1366) R^(D143) R^(D196) L_(C1205) R^(D10) R^(D197) L_(C1259) R^(D55) R^(D197) L_(C1313) R^(D37) R^(D197) L_(C1367) R^(D143) R^(D197) L_(C1206) R^(D10) R^(D198) L_(C1260) R^(D55) R^(D198) L_(C1314) R^(D37) R^(D198) L_(C1368) R^(D143) R^(D198) L_(C1207) R^(D10) R^(D199) L_(C1261) R^(D55) R^(D199) L_(C1315) R^(D37) R^(D199) L_(C1369) R^(D143) R^(D199) L_(C1208) R^(D10) R^(D200) L_(C1262) R^(D55) R^(D200) L_(C1316) R^(D37) R^(D200) L_(C1370) R^(D143) R^(D200) L_(C1209) R^(D10) R^(D201) L_(C1263) R^(D55) R^(D201) L_(C1317) R^(D37) R^(D201) L_(C1371) R^(D143) R^(D201) L_(C1210) R^(D10) R^(D202) L_(C1264) R^(D55) R^(D202) L_(C1318) R^(D37) R^(D202) L_(C1372) R^(D143) R^(D202) L_(C1211) R^(D10) R^(D203) L_(C1265) R^(D55) R^(D203) L_(C1319) R^(D37) R^(D203) L_(C1373) R^(D143) R^(D203) L_(C1212) R^(D10) R^(D204) L_(C1266) R^(D55) R^(D204) L_(C1320) R^(D37) R^(D204) L_(C1374) R^(D143) R^(D204) L_(C1213) R^(D10) R^(D205) L_(C1267) R^(D55) R^(D205) L_(C1321) R^(D37) R^(D205) L_(C1375) R^(D143) R^(D205) L_(C1214) R^(D10) R^(D206) L_(C1268) R^(D55) R^(D206) L_(C1322) R^(D37) R^(D206) L_(C1376) R^(D143) R^(D206) L_(C1215) R^(D10) R^(D207) L_(C1269) R^(D55) R^(D207) L_(C1323) R^(D37) R^(D207) L_(C1377) R^(D143) R^(D207) L_(C1216) R^(D10) R^(D208) L_(C1270) R^(D55) R^(D208) L_(C1324) R^(D37) R^(D208) L_(C1378) R^(D143) R^(D208) L_(C1217) R^(D10) R^(D209) L_(C1271) R^(D55) R^(D209) L_(C1325) R^(D37) R^(D209) L_(C1379) R^(D143) R^(D209) L_(C1218) R^(D10) R^(D210) L_(C1272) R^(D55) R^(D210) L_(C1326) R^(D37) R^(D210) L_(C1380) R^(D143) R^(D210) L_(C1219) R^(D10) R^(D211) L_(C1273) R^(D55) R^(D211) L_(C1327) R^(D37) R^(D211) L_(C1381) R^(D143) R^(D211) L_(C1220) R^(D10) R^(D212) L_(C1274) R^(D55) R^(D212) L_(C1328) R^(D37) R^(D212) L_(C1382) R^(D143) R^(D212) L_(C1221) R^(D10) R^(D213) L_(C1275) R^(D55) R^(D213) L_(C1329) R^(D37) R^(D213) L_(C1383) R^(D143) R^(D213) L_(C1222) R^(D10) R^(D214) L_(C1276) R^(D55) R^(D214) L_(C1330) R^(D37) R^(D214) L_(C1384) R^(D143) R^(D214) L_(C1223) R^(D10) R^(D215) L_(C1277) R^(D55) R^(D215) L_(C1331) R^(D37) R^(D215) L_(C1385) R^(D143) R^(D215) L_(C1224) R^(D10) R^(D216) L_(C1278) R^(D55) R^(D216) L_(C1332) R^(D37) R^(D216) L_(C1386) R^(D143) R^(D216) L_(C1225) R^(D10) R^(D217) L_(C1279) R^(D55) R^(D217) L_(C1333) R^(D37) R^(D217) L_(C1387) R^(D143) R^(D217) L_(C1226) R^(D10) R^(D218) L_(C1280) R^(D55) R^(D218) L_(C1334) R^(D37) R^(D218) L_(C1388) R^(D143) R^(D218) L_(C1227) R^(D10) R^(D219) L_(C1281) R^(D55) R^(D219) L_(C1335) R^(D37) R^(D219) L_(C1389) R^(D143) R^(D219) L_(C1228) R^(D10) R^(D220) L_(C1282) R^(D55) R^(D220) L_(C1336) R^(D37) R^(D220) L_(C1390) R^(D143) R^(D220) L_(C1229) R^(D10) R^(D221) L_(C1283) R^(D55) R^(D221) L_(C1337) R^(D37) R^(D221) L_(C1391) R^(D143) R^(D221) L_(C1230) R^(D10) R^(D222) L_(C1284) R^(D55) R^(D222) L_(C1338) R^(D37) R^(D222) L_(C1392) R^(D143) R^(D222) L_(C1231) R^(D10) R^(D223) L_(C1285) R^(D55) R^(D223) L_(C1339) R^(D37) R^(D223) L_(C1393) R^(D143) R^(D223) L_(C1232) R^(D10) R^(D224) L_(C1286) R^(D55) R^(D224) L_(C1340) R^(D37) R^(D224) L_(C1394) R^(D143) R^(D224) L_(C1233) R^(D10) R^(D225) L_(C1287) R^(D55) R^(D225) L_(C1341) R^(D37) R^(D225) L_(C1395) R^(D143) R^(D225) L_(C1234) R^(D10) R^(D226) L_(C1288) R^(D55) R^(D226) L_(C1342) R^(D37) R^(D226) L_(C1396) R^(D143) R^(D226) L_(C1235) R^(D10) R^(D227) L_(C1289) R^(D55) R^(D227) L_(C1343) R^(D37) R^(D227) L_(C1397) R^(D143) R^(D227) L_(C1236) R^(D10) R^(D228) L_(C1290) R^(D55) R^(D228) L_(C1344) R^(D37) R^(D228) L_(C1398) R^(D143) R^(D228) L_(C1237) R^(D10) R^(D229) L_(C1291) R^(D55) R^(D229) L_(C1345) R^(D37) R^(D229) L_(C1399) R^(D143) R^(D229) L_(C1238) R^(D10) R^(D230) L_(C1292) R^(D55) R^(D230) L_(C1346) R^(D37) R^(D230) L_(C1400) R^(D143) R^(D230) L_(C1239) R^(D10) R^(D231) L_(C1293) R^(D55) R^(D231) L_(C1347) R^(D37) R^(D231) L_(C1401) R^(D143) R^(D231) L_(C1240) R^(D10) R^(D232) L_(C1294) R^(D55) R^(D232) L_(C1348) R^(D37) R^(D232) L_(C1402) R^(D143) R^(D232) L_(C1241) R^(D10) R^(D233) L_(C1295) R^(D55) R^(D233) L_(C1349) R^(D37) R^(D233) L_(C1403) R^(D143) R^(D233) L_(C1242) R^(D10) R^(D234) L_(C1296) R^(D55) R^(D234) L_(C1350) R^(D37) R^(D234) L_(C1404) R^(D143) R^(D234) L_(C1243) R^(D10) R^(D235) L_(C1297) R^(D55) R^(D235) L_(C1351) R^(D37) R^(D235) L_(C1405) R^(D143) R^(D235) L_(C1244) R^(D10) R^(D236) L_(C1298) R^(D55) R^(D236) L_(C1352) R^(D37) R^(D236) L_(C1406) R^(D143) R^(D236) L_(C1245) R^(D10) R^(D237) L_(C1299) R^(D55) R^(D237) L_(C1353) R^(D37) R^(D237) L_(C1407) R^(D143) R^(D237) L_(C1246) R^(D10) R^(D238) L_(C1300) R^(D55) R^(D238) L_(C1354) R^(D37) R^(D238) L_(C1408) R^(D143) R^(D238) L_(C1247) R^(D10) R^(D239) L_(C1301) R^(D55) R^(D239) L_(C1355) R^(D37) R^(D239) L_(C1409) R^(D143) R^(D239) L_(C1248) R^(D10) R^(D240) L_(C1302) R^(D55) R^(D240) L_(C1356) R^(D37) R^(D240) L_(C1410) R^(D143) R^(D240) L_(C1249) R^(D10) R^(D241) L_(C1303) R^(D55) R^(D241) L_(C1357) R^(D37) R^(D241) L_(C1411) R^(D143) R^(D241) L_(C1250) R^(D10) R^(D242) L_(C1304) R^(D55) R^(D242) L_(C1358) R^(D37) R^(D242) L_(C1412) R^(D143) R^(D242) L_(C1251) R^(D10) R^(D243) L_(C1305) R^(D55) R^(D243) L_(C1359) R^(D37) R^(D243) L_(C1413) R^(D143) R^(D243) L_(C1252) R^(D10) R^(D244) L_(C1306) R^(D55) R^(D244) L_(C1360) R^(D37) R^(D244) L_(C1414) R^(D143) R^(D244) L_(C1253) R^(D10) R^(D245) L_(C1307) R^(D55) R^(D245) L_(C1361) R^(D37) R^(D245) L_(C1415) R^(D143) R^(D245) L_(C1254) R^(D10) R^(D246) L_(C1308) R^(D55) R^(D246) L_(C1362) R^(D37) R^(D246) L_(C1416) R^(D143) R^(D246)

wherein R^(D1) to R^(D246) have the following structures:


15. The compound of claim 1, wherein the compound is selected from the group consisting of:


16. The compound of claim 11, wherein the compound has the Formula II:

wherein: M¹ is Pd or Pt; moieties E and F are each independently monocyclic or polycyclic ring structure comprising 5-membered and/or 6-membered carbocyclic or heterocyclic rings; Z¹, Z², X^(3′), and X^(4′) are each independently C or N; K, K¹, and K² are each independently selected from the group consisting of a direct bond, O, and S, wherein at least two of them are direct bonds; L¹, L², and L³ are each independently selected from the group consisting of a single bond, absent a bond, O, S, CR′R″, SiR′R″, BR′, and NR′, wherein at least one of L¹ and L² is present; R^(E) and R^(F) each independently represents zero, mono, or up to a maximum allowed number of substitutions to its associated ring; each of R′, R″, R^(E), and R^(F) is independently a hydrogen or a substituent selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile, isonitrile, sulfanyl, and combinations thereof; and two adjacent R^(A), R^(B), R^(C), R^(E), and R^(F) can be joined or fused together to form a ring where chemically feasible.
 17. An organic light emitting device (OLED) comprising: an anode; a cathode; and an organic layer disposed between the anode and the cathode, wherein the organic layer comprises a compound comprising a first ligand L_(A) of Formula I

wherein: ring C is a 5-membered or 6-membered carbocyclic or heterocyclic ring; each of X¹ to X⁸ is independently C or N; one of X¹ to X⁴ is C and is connected to ring C, and one of X¹ to X⁴ is N and is coordinated to a metal M; Y is selected from the group consisting of O, S, Se, NR′, BR′, BR′R″, CR′R″, SiR′R″, GeR′R″, C═O, C═CRR′, and C═NR′; K is selected from the group consisting of a direct bond, O, and S; each of R^(A), R^(B), and R^(C) independently represents mono to the maximum allowable substitution, or no substitution; each R′, R″, R^(A), R^(B), and R^(C) is independently a hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, boryl, arylalkyl, alkoxy, aryloxy, amino, silyl, germyl, selenyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; at least one of R^(A) or R^(B) comprises an electron-withdrawing group; at least one of R^(B) is a cyclic group; L_(A) is coordinated to a metal M via the indicated dashed lines; metal M is selected from the group consisting of Os, Ir, Pd, Pt, Cu, Ag, and Au; L_(A) can be joined with other ligands to comprise a tridentate, tetradentate, pentadentate, and hexadentate ligand; and any two substituents can be joined or fused to form a ring.
 18. The OLED of claim 17, wherein the organic layer further comprises a host, wherein host comprises at least one chemical moiety selected from the group consisting of triphenylene, carbazole, indolocarbazole, dibenzothiophene, dibenzofuran, dibenzoselenophene, 5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracene, aza-triphenylene, aza-carbazole, aza-indolocarbazole, aza-dibenzothiophene, aza-dibenzofuran, aza-dibenzoselenophene, and aza-(5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracene).
 19. The OLED of claim 18, wherein the host is selected from the group consisting of:

and combinations thereof.
 20. A consumer product comprising an organic light-emitting device (OLED) comprising: an anode; a cathode; and an organic layer disposed between the anode and the cathode, wherein the organic layer comprises a compound comprising a first ligand L_(A) of Formula I

wherein: ring C is a 5-membered or 6-membered carbocyclic or heterocyclic ring; each of X¹ to X⁸ is independently C or N; one of X¹ to X⁴ is C and is connected to ring C, and one of X¹ to X⁴ is N and is coordinated to a metal M; Y is selected from the group consisting of O, S, Se, NR′, BR′, BR′R″, CR′R″, SiR′R″, GeR′R″, C═O, C═RR′, and C═NR′; K is selected from the group consisting of a direct bond, O, and S; each of R^(A), R^(B), and R^(C) independently represents mono to the maximum allowable substitution, or no substitution; each R′, R″, R^(A), R^(B), and R^(C) is independently a hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, boryl, arylalkyl, alkoxy, aryloxy, amino, silyl, germyl, selenyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; at least one of R^(A) or R^(B) comprises an electron-withdrawing group; at least one of R^(B) is a cyclic group; L_(A) is coordinated to a metal M via the indicated dashed lines; metal M is selected from the group consisting of Os, Ir, Pd, Pt, Cu, Ag, and Au; L_(A) can be joined with other ligands to comprise a tridentate, tetradentate, pentadentate, and hexadentate ligand; and any two substituents can be joined or fused to form a ring. 